Arkiv för februari, 2011

Collaboration Between Enterprises and NGOs

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Today I participated in a discussion regarding collaborations between enterprises and NGOs (Non-Governmental Organizations). The meeting was arranged by CSR Sweden and Charity Rating.

Marianne Bogle och Camilla Backström

Marianne Bogle och Camilla Backström

After the introduction by Marianne Bogle from CSR Sweden and Camilla Backström from Charity Rating a presentation by Lovisa Cottrell, from Sponsoir Insight, followed. Lovisa gave us some highlights from a study they have performed regarding companies’ CSR initiatives. 240 companies have responded to a range of questions and the answers have also been followed-up through interviews.

Lovisa Cottrell

Lovisa Cottrell

Lovisa presented some of the interesting results from the study, e.g.:

Drivers for CSR initiatives:

Building the brand (79% of responders that work with CSR said YES)

Build employee loyalty (72%)

Competence development (65%)

Risk management (55%)

Product development (32%)

“Give back to society” (16%)

Others (12%)

Areas for collaboration with NGOs:

Children (49% of responders that have a collaboration with an NGO said YES)

Environment (42%)

Aid / Charity (37%)

Sports (33%)

Health (29%)

Cultur (23%)

Human Rights (22%)

Research (20%)

Others (12%)

After the introduction and the presentation by Lovisa, a panel discussion followed. The panellists were Lovisa, myself, Vivianne Gillman (Connecta), and Erik Zachrison (FRII Insamlingsrådet). The discussion was moderated by Kaj Török from Futerra.

We had a good discussion, with a lot of interaction with the audiance. I came back time after time to one of my “key messages” when it comes to collaboration between enterprises and NGOs. The collaboration has to be driven by a “business reason”. All our CSR-initiatives, including of course NGO-collaborations, are integrated into our business strategies. A part of our operations. In the discussions we used expressions such as “driven by the brain” in contrast to “driven by the heart”. As you know if you have followed me here on the blog (see for instance the blog post from March 29 last year) I feel strongly that in my “professional life” brain shall govern when we decide on a collboration wiht an NGO, wheras in my private life I am very often guided by my heart when I decide to which organization I make my own donations.

Another topic we discussed was the need for NGOs to become more “professional”. It is, and may become even more so in the future, a competetive edge for an NGO to act very “professionally” in the contacts with companies, and to develop processes in order to better report back on goals, objectives and deliverables. However, it is important, stressed for instance very nicely by Erik Z, that NGOs do not “loose their heart” in their ambition to become more “professional”. There are of course good reason why there is, and probably should be, differences in drivers for NGOs and enterprises…

A good discussion and I look forward to the coming events in this so called “SAM series”. Keep your eyes open for events on March 15, April 7, and April 28.

Postat av Bengt Mattson

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Green Criteria and Green Incentives

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As you are aware of from my blog posts last week (Feb 18 first post and Feb 18 second post) and the one from this Monday, there has been a lot of discussions on the Swedish Radio regarding releases from pharmaceutical manufacturing in India. Today there was a new news item on the radio news show (”the Echo” or in Swedish Ekot). I refer to this news item as “Ekot 8″ in alignment with the numbering from last week. The translation has been made by the LIF office (LIF is the Swedish association of the research based pharmaceutical industry) using “Google Translate”.

Ekot 8: “Stricter environmental requirements for medical manufacturing” (Radio: “The Echo”, Wed 23 Feb)

Following the revelation that the manufacture of pharmaceutical compounds causes resistance bacteria to spread in India and globally, the Swedish rules will be tightened for drugs that Swedish counties buy.

For the first time, the environmental impact of manufacturing will be inspected before the county buy drugs, “says Professor Åke Wennmalm, former Environmental Director of Stockholm County Council.

- The idea is that we should have a system that includes manufacturing variables, that is, emissions, quality and so on, and also the working conditions and other human aspects for those involved with production, “says Åke Wennmalm.

To date, the exchange system of medicines in pharmacies requires that the cheapest drug copy has to be sold. The system annually saves seven billion SEK for the state of Sweden. To the cost of a deteriorating environment around the Indian factories that account for nearly half of the production of drug compounds sold in Sweden. A sufficiently effective treatment of wastewater will result in higher prices for the products.

Since an increasing number of alarms comes from India - both of very high levels of antibiotics in wastewater from manufacturing, and of unexplained illnesses suffered by the residents around the plants - currently more and more voices are being raised for an environmental classification of medicines.

There is already a voluntary Swedish system where medicines environmental impact is reviewed. Manufacturers are asked what emissions their products cause. So far it only contains emissions to wastewater after use, but now starts also the examination of how manufacturing affects the environment, “says Åke Wennmalm.

- I think we can have a sort of protocol for how that review will function, maybe this year. Then, it must be applied, so after a few years I think we will begin to see results from it.

When can I, as a patient, get medication manufactured in an environmentally friendly manner?

- At the best, you can get it within a year, because there are certainly drugs that already meet these requirements that we are considering for new drugs. Many drugs, however, obviously will not reach them, or most of them will not, “says Åke Wennmalm, professor of clinical physiology and former Environment Director, Stockholm County Council.

 

When Åke Wennmalm talks about potential alterations in the enviromental classification scheme of pharmaceutical substances on fass.se, he refers to a meeting with the “environmental classification working group” that was held in late January at the LIF-office. Read my summarizing minutes of the meeting at the following link (the discussion about the classification scheme is presented in the last part of the blog post).

We did all agree that it is worth looking into expanding the classification scheme to also include other criteria, such as manufacturing conditions for instance. But how it will evolve no one can know for sure. Let me quote my own words from the January 28 blog post:

“And what is a “green criteria”, based on which a products and/or a company could be branded “green”? Of course one critical aspect is the environmental risk assessment of the substance itself, but additional aspects could be manufacturing releases and emissions, packaging solutions, transport patterns and so on. In the meeting yesterday, Åke Wennmalm talked about his ideas regarding a “crash test” of pharmaceuticals. Read more about his ideas on via this link to Läkemedelsvärlden. Since the criteria must be possible to evaluate objectively by authorities such as Swedish MPA and TLV (in English: The Dental and Pharmaceutical Benefits Agency) in order for them to be able to present “green incentives” to industry we of course need to find ways to present enviromental information in an “science based, clear and concise manner”. One proposal worth to look further into was presented by Staffan Castensson at the meeting: Water footprint. Staffan participates on behalf of MPA in a working group focused on the development of an international standard in the area (i.e. ISO 14046).
We have a long way to go, but the process has been initiated. And I am proud to say that, as for the environmental classification scheme development, LIF has decided to be in a driving seat.”

I hope to see a fairly rapid development here, but as long as there are no real incentives presented, I have personally hard to believe that changes will come… If the government and/or the County Councils only look for the lowest possible price, the changes are not likely to come and to be spread all over the industry…

Postat av Bengt Mattson

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Follow-up of Last Week’s Reports on API Releases in India

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Friday February 18, I gave my reflections in two blog posts (blog post No 1 and blog post No 2) to the news aired last week on Swedish Radio regarding releases of pharmaceutical substances in India. Several news papers (e.g. DN, NyTeknik, KemivärldenBiotech) have now picked up the story from Swedish Radio and give their comments. The discussions are also on-going in the blogoshere, e.g. Ethel Forsberg, former Director General at Swedish Chemicals Agency, gives here comments at MiljöAktuellt’s blog. And you can also find the comments of Ingrid Stenberg at Läkemedelsvärlden.se.

In general I feel that the discussions and the different comments are balanced and helpful in describing not only the problem (in focus in the articles in NyTeknik and KemivärldenBiotech for instance) but also potential solutions (in focus for DN and Läkemedelsvärlden). I would like to give two comments on this:

1) I think it is important to add to the picture that “industry’s search for low costs” as decribed by Ethel Forsberg in the MiljöAktuellt’s blog is not only industry’s search, but actually something very strongly driven by society. I guess everyone is familiar with the generic reform, where pharmacies are obliged to substitute the prescribed pharmaceutical product with the cheapest generic (low-cost copy). As long as society only focus price, and do not add in any other criteria in addition to therapeutic effect, companies that invests in environmental protection will actually lose competetive edge… We need to improve the pricing and re-imbursement system, including the generic reform, by adding “green incentives”. Read more regarding “green incentives” in my blogpost from Feb 8 (see especially “step 4″).

2) DN favours a solution based on regulatory initiatives. Specifically the inclusion of environmental requirements into GMP (Good Manufacturing Practice). Read more about the wotk on this issue in my blogpost from Jan 5, 2011. Läkemedelsvärlden however decribes another option which I personally believe is a faster track than alterations to GMP. Coming back to my first comment again: As long as society only focus price, and do not add in any other criteria in addition to therapeutic effect, companies that invests in environmental protection will actually lose competetive edge… We need to improve the pricing and re-imbursement system, inclusing the generic reform, by adding “green incentives”.

Looking forward to a continuation of the debate!

Postat av Bengt Mattson

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More on releases in India on the radio

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I gave my reflections earlier today here on the blog to the last few days of reports on Swedish Radio, mainly in “the Echo” (i.e. “Ekot” in Swedish), regarding releases of active pharmaceutical ingredients from manufacturing in India. After that, additional reports have been aired:

Ekot 7“: “Where drugs are produced is a secret”

The consumer who wants to buy an environmentally friendly medicine will get problems. The Echo has just reported on how the environment is destroyed in the Indian Hyderabad because of medical manufacturing. But neither the MPA or trade associations for pharmaceutical companies think the time is here to tell where each individual drug is manufactured. Meanwhile, many customers want to have a choice. 

- Absolutely. In the case of pharmaceuticals, I think we know too little, and it is so difficult to find out, while we know so much about light bulbs and everything else in our everyday environment, “says Helen Rehn.

- It would be great if you could get information about it, kind of like when you buy a plane ticket, where you can always see the environmental impact. Then, you could make a conscious choice, “says Sara Åsberg.

Would you care if such information existed?

- Absolutely!

Those who today want to know whether a drug is manufactured in an environmentally sound manner has no way find out. Information on how and where drugs are produced are kept secret, both by companies and by the MPA. Despite the reports of environmental damage related to the manufacture of medicines. In Hyderabad, the Indian medicine factories caused an environmental disaster. In surrounding lakes, there is as much antibiotic as humans have in their blood during an ongoing treatment. But that is no reason to tell where a drug comes from, thinks Kenneth Nyblom of Generic Association, which is the trade association for the companies that produce cheap generic copies.

- The question is whether it is the right way to go and if it really helps the environment. I think we should be working on a general rise in standards. That would most benefit the environment.

Instead of that companies themselves will tell you where drugs are produced, the Generics Association wants stricter rules on an international level. Something that MPA estimates can take ten years to complete. Also the MPA has information on which factories producing medicines. But this information cannot be disclosed, was the news when the echo requested the documents.

- We have information on where companies produce their drugs, but that information is in the current situation classified as secret, “says Charlotte Unger, who is environmental manager at the MPA.

 

There was also a live debate in “Studio 1” (aired roughly at 17.30) presented as follows:

“Listen to a debate in Studio One between Cecilia Marlow, president of the pharmacy Kronans Droghandel and Anders Blanck, vice president of the Pharmaceutical Association, LIF. Also hear Mona Hambraeus from “the Echo” about the damage that Swedish pharmaceutical manufacturing contribute to in India.”

Both Cecilia and Anders said they were positive to try to make changes in order to enable consumers to make “green choices”. Anders however also described some obstacles that need to be managed in order for such choices to be possible. This is well inline with LIF’s ideas I have described earlier about making changes not only within international regulations such as GMP, but actually work within the Swedish “pricing and reimbursement systems”. If people want to make “green choices” they should be able to do so. But where are the “green incentives” in the systems enabling this?

I hope the discussions from this week will help drive the debate on “green criteria” and “green incentives”, in addition to the work that Swedish MPA has been commissioned already to further investigate changes in the GMP-regulation.

If you would like additional reading on this matter I also recommend you to read Agneta Borgström’s article in the paper “Vi” (Number 2, 2011, pages 30 - 37). It is always valuable I think to get as many different views and perspectives on issues as possible when you should develop your own opinion on an issue. The article in “Vi” is pretty much the same material that has been aired by “the Echo” over the last few days.

Postat av Bengt Mattson

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Releases of API from Pharmaceutical Manufacturing in India

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There has been a lot of discussions in Swedish Radio News “Ekot” (translated into English it would be “the Echo”), this week regarding releases of active pharmaceutical ingredients (API) from pharmaceutical manufacturing in India. For me it has been a very different week for completely other reasons. My father passed away the day before yesterday after having a stroke last Friday. Hence, I have not taken part in this week’s discussions on API releases. Nevertheless, I would like to give my personal reflections to the “Ekot-news”. Below follows first a very general comment and then a translation of 6 news articles that have been aired by Ekot this week. After that I give my personal reflections.

The topic as such is not new. We have all been aware of the situation in Patancheru, in the Hyderabad area in India, ever since the first publication on the issue by Cecilia de Pedro (AstraZeneca), Joakim Larsson (Sahlgrenska Akademin, Göteborgs Universitet) and Nicklas Paxeus (Gryaab AB) back in 2007. It has been one of the issues that I have written the most blog posts on during the last 3 years. Read for instance my blog post from Aug 16, 2010, where you will also find links to several of the other blog posts.

The different “Ekot-news” from the passed few days are summarized below. Translations to English is made by the LIF-office (LIF, the association of the reasearch based pharma industry in Sweden) using “Google Translation”:

Ekot 1. “Swedish pharmaceutical producers contribute to environmental disaster”

A growing part of our medicines are manufactured in low cost countries, and India has emerged as a major producer. But pharmaceutical companies have caused an environmental disaster outside India Hyderabad, and “the echo” can now reveal that several of the largest suppliers to the Swedish market is just there.  Anil Dayak from the local environmental organization Gamana says that many companies dump their toxic waste directly into lakes and land and that it is constantly increasing. A few years ago, researchers from Gothenburg found massive release of drugs from the pharmaceutical industry in Hyderabad, India. Massive amounts of eleven different drug substances were found in rivers and drinking water wells - heart medicines, blood pressure medicines, allergy medications and antidepressants. But worst of all was the antibiotics - there were more antibiotics in the rivers than humans have in their blood during an ongoing treatment. In the factories drugs are manufactured which are sold worldwide, also in Sweden. When “the Echo” asked the MPA for data on the origins of Swedish medicines, it emerged that four of the ten largest manufacturers of active ingredient to the Swedish medicines is in Hyderabad, India. But the MPA makes no environmental controls on drugs sold in Sweden. “It would be against the rules of EU”, says environmental director Charlotte Unger.

- We have low requirements concerning the production. There are no limits saying this much is OK to emit, antibiotics for example, and that is why the government has given us a mission to see how we can change the laws of EU to include also that, “says Charlotte Unger.

According to “the Echo”, it is likely that the companies that supply medicines to Sweden also contributes to environmental disaster in India. The local environmental authority in Hyderabad confirmed that at least two of the major Swedish suppliers send their wastewater to the widely criticized general treatment plant in the area. Every day, the waste-water treatment plant let out 44 kilograms of antibiotics in nature, according to Swedish researchers who carried out measurements on site. There have been no studies of how drugs emissions affect human health. But a Greenpeace report speaks of a greatly increased risk of cancer and heart disease in the villages around the medicine factories. Anil Dayak from Gamana environmental organization says that the problems were big already five years ago, but now it’s worse because of the high demand for drugs.

Ekot 2. ”We export our environmental problems”

New figures from the MPA shows that nearly half of the cheap generic pharmaceuticals that Swedes consume are produced in factories in India. Medicine becomes less expensive, but at the cost of severe environmental problems abroad, “says Charlotte Unger, environmental manager at the MPA.

- The biggest problems are that we do something that is not acceptable, that we export our environmental problems to another country, “says Charlotte Unger, environmental manager at the MPA.

Anil Dayak on the Indian environmental organization Gamana in Hyderabad, confirms the picture of a gigantic environmental problem. Pharmaceutical companies dump waste straight into the wild.

- The factories dump their waste in lakes and in the wild, and that procedure is now increasing.

It is mainly the cheap drug copies, produced in low cost countries. Nearly half, or 46 percent, of the active ingredients in the substituted medicines we get in the pharmacies are manufactured in India showed the MPA databases that echo requested. There are currently no environmental requirements for pharmaceuticals. Karin Johansson, State Secretary at the Ministry of Health agrees that there needs to be changed.

- We’ve asked the MPA to submit concrete proposals on the amendments on the regulations that exist regarding drug production, to be more demanding.

Today one cannot impose environmental requirements, is that a problem?
- Yes, of course, “said Karin Johansson.

Most operators, industry, authorities and politicians, agree that we have to change the global rules for the manufacture of pharmaceuticals, so they not only ensure human health, but, also the environment in the manufacturing countries. But the changing global regulatory framework takes time, “says Charlotte Unger at the MPA.

- The vast majority of the work is to put the issue on the table, it is important and then it takes less time to change the laws.
And approximately how long?
- I think one can expect between five to ten years.

Ekot 3. “The state saves billions on environmental scandal in India”

The Swedish exchange system for pharmaceuticals, forcing pharmacies to dispatch the cheapest medicines, may contribute to serious environmental damage from production in India for example. The extremely cheap production and poor treatment of wastewater from factories makes drinking water polluted and people ill. But at the “Dental and Pharmaceutical Reimbursement Agency (TLV)” Magnus Thyberg said that they hitherto have not been allowed to take environmental considerations.

- The state subsidy system does not account for the environmental aspects of generics, but in essence there is no knowledge of which medicines are environmentally friendly, said Magnus Thyberg, TLV.

The Swedish system of generic replacement, which means that the expensive original drugs are replaced by cheap copies in the pharmacy, entail high economic contribution to the state. More than seven billion per year, according to the calculations, and according to recent studies, Sweden has the lowest prices on generic versions when comparing 18 European countries. But the production of the cheap medicines causes severe damage to the environment around the factories outside the Indian city of Hyderabad, and people in the area are sick. Several of those factories produce substances for drugs sold in Sweden. And it is the low price that is most important when the authority TLV select between different medications. In the case of new medicines, TLV may consider environmental issues, but it has not been done, “said Magnus Thyberg.

- If a company could argue that it received a higher benefit and lower cost if you had a minor impact on the environment, we can take that into account under the legislation we have. But it requires companies to demonstrate this connection for us and argue for it, and it has not yet been done by any company.

When you created the generics system without regard to the environment, was it so very successful?

- All countries in the world actually have tried systems that, when a patent has expired, attempt to use market competition, and environmental issues were not something that was discussed and not in any country that I know of, “said Magnus Thyberg, TLV.

Ekot 4. “Cheap drugs cause resistant bacteria“

In India, soaring levels of resistant bacteria have been found in the environment around the drug factories supplying cheap drugs to countries such as Sweden. A new Swedish study now shows that the bacteria in soil and water are becoming more resistant to antibiotics.

- We have shown that the major release of antibiotics that we have previously seen is at production sites in India, also leads to much greater resistance, says Dr. Joakim Larsson, Göteborg University.

Joakim Larsson and his colleagues took samples of the environment around the Indian pharmaceutical factories outside Hyderabad. Here are substances manufactured for drugs that are sold worldwide, also in Sweden. Four of the ten largest suppliers to the Swedish market is here. But production causes serious environmental problems. The treatment plant receives wastewater factories and emits 44 kg of antibiotics every day. The new study, published in the scientific journal PLoS One, shows that the suspicions of an increased antibiotic resistance in bacteria in the environment is confirmed.

The bacteria’s resistance genes are at least 100 times as common in the area around the Indian Hyderabad as in Sweden, “said Joakim Larsson, Göteborg University.
- It means that there is a risk that the genes conferring resistance of the bacteria might be spread to bacteria that cause diseases.

The researchers findings around the factories are not the type of resistant bacteria we have problems with in hospitals today. Instead, it’s bacteria that occurs naturally in the environment, which has become significantly resistant. No one knows how easily the resistance genes detected in India could spread to bacteria that provide human diseases, but the risk exists and is worrying, “said Joakim Larsson.

- If it happens it is very serious. We have a big problem of antibiotic resistance today and the World Health Organization classifies it as one of the three greatest threats to public health.

Ekot 5. “Swedish treatment plants cannot handle all the antibiotics”

Indian pharmaceutical emissions worries scientists, but not even Swedish sewage treatment plants reach a high standard. Swedish treatment plant is not able to clean synthetic antibiotics, “says Professor Otto Cars, chairman of the network ReAct.

The Echo has reported on the major problems of emissions from the Indian pharmaceutical manufacturing. The countryside around the Indian plant outside Hyderabad contain not only antibiotics but also environmental bacteria that become resistant. The companies have not managed to clean up their emissions sufficiently. But neither Swedish sewage treatment plants are able to clean off synthetic antibiotics, it says Professor Otto Cars, chairman of the network ReAct.

- Some of these antibiotics which are synthetic cannot be eliminated with our methods either, although of course here in Sweden it is a much less quantitative problem, “says Otto Cars.

The Swedish researchers report presented today shows that the bacteria in soil and water around the Indian plant has become resistant. That as a result of high concentrations of drugs in wastewater from pharmaceutical factories in the area. Researchers have investigated the bacteria that occurs naturally in the environment, but they may be able transfer their resistance to pathogenic bacteria. The researcher Joakim Larsson is concerned.

- If it happens it is very serious. We have a big problem of antibiotic resistance in day and the World Health Organization classifies it as one of the three greatest threats to public health, “said Joakim Larsson.

Professor Otto Cars, who has worked on issues of antibiotic resistance, sees the emissions from the manufacturing of medicines as yet another threat to the antibiotics that are still effective. - It’s hard to say, in quantitative terms, how big the problem is in relation to the massive misuse of antibiotics in both human and veterinary medicine appearing everywhere.

- All emissions and all misuse of antibiotics is necessary to try to reduce. The risk is that what is emitted this way will come back in the cycle through the water, soil, animals, people and food, “says Otto Cars.

Ekot 6. “They choose cheap production despite environmental problems”

More and more pharmaceutical companies outsource their manufacturing to contract for low cost countries. AstraZeneca and Pfizer are among those who have signed an agreement in Indian Hyderabad, despite the fact that pharmaceutical plants emit very large quantities of drugs into the environment. For Pfizer’s part a low price was an important factor, and we were well aware of environmental problems in the area when signing up for a few years ago, says John Walde, Senior Director at Pfizer in Sweden.

- Yes, we did. We knew them and had our eyes fully open to it. We reasoned that it is better to be in place and try to influence from within, in cooperation with our suppliers than to refuse them.

The Echo has just told you about how pharmaceutical manufacturers in India Hyderabad emit very large quantities of pharmaceuticals in the environment. Swedish researchers have measured sky-high levels of antidepressants, allergy medications and antibiotics in lakes and drinking water wells.

The land and water has also a sharp increase in antibiotic-resistant bacteria, and people in the area have health problems, “says Joakim Larsson of the University of Gothenburg, which was the first to reveal the emissions.

- I had pain in my chest by walking along such a lake after a few minutes, and it stayed all day because of the chemical vapors that came up from the surface. It is an extremely polluted environment, “he says.

From the company Aurobindo Pharma in this area, Pfizer is buying antidepressant drugs and diabetes drugs. Also AstraZeneca has contracts for more than 20 medicines with the same company, and also with Divis Laboratories to manufacture the active ingredient. Both Aurobindo and Divis is connected to the criticized treatment plant in Hyderabad, which emits the drugs in the environment.

AstraZeneca sais that a thorough environmental review was conducted before the Indian contracts were written. In the same time you cannot promise that the environment is not affected, says the company responsible for contracting out the active ingredient, Nicklas Westerholm.

- We cannot guarantee it 100 percent because some 90 plants is treated in the same treatment plant. However, we are working very closely to the suppliers we have chosen and ensure that they continuously improve their processes and have an eye on their emissions.

If you cannot guarantee it 100 percent, why have you chosen this vendor?
- We have done the same control of this provider as of all others, and they meet our internal requirements, “said Nicklas Westerholm.

 

The discussion at Ekot has of course resulted in attention also from other media representatives. One of my favourite news letters, MiljöRapporten Direkt, from MiljöRapporten had the following comment today (in Swedish), based on an interview with Richard Bergström, Managing Director of LIF:

“Fortsatt uppmärksamhet kring indiska utsläpp av läkemedelsrester

Sveriges Radio Ekot fortsätter att uppmärksamma de sedan några år kända problemen vid tillverkning av aktiva läkemedelsrester i Indien. Ekot tar upp det faktum att både Pfizer och AstraZeneca använder sig av leverantörer som kan kopplas till utsläppen till reningsverk i Hyderabad. Frågan uppmärksammades första gången av den svenska forskaren Joakim Larsson.

Richard Bergström, vd på branschorganisationen Lif, de forskande läkemedelsföretagen, hoppas på en miljöcertifiering av läkemedel för att förbättra utsläppsreningen och säger att det är svårt för läkemedelsföretagen att byta leverantörer.

– Vi känner till problemen men i dag finns inga drivkrafter för underleverantörerna att investera i grön teknologi. Läkemedelsbolagen kan inte bara starta upp en ny anläggning heller eftersom det tar lång tid att få alla tillstånd och godkännande. Det som behövs nu är bland annat ett miljöcertifieringssystem som gör det ekonomiskt lönsamt att satsa på hållbart tillverkade läkemedel, säger han till MiljöRapporten Direkt.”

So what are my reflections on all this?

First of all, I would say that all stakeholders are aware of and worried by the situation. Everyone understands that actions are needed. Some stakeholders have a preference for regulatory initiatives, others for market driven initiatives. Probably we will see some kind of a mix of both types of initiatives. The Swedish MPA continue their work to evaluate the possibility to include environmental requirements into GMP (Good Manufacturing Practice) as proposed in their report on the issue from Dec 2009. As you know if you have followed my blog, I however believe market driven initiatives such as “green incentives” will give faster results and should therefore be evaluated in parallel to regulatory initiatives. Read my blog post from Feb 8 called “4 steps to a sustainable use of pharmaceuticals” and focus upon “step 4″.

It is a good thing that the pharmaceutical industry is present in countries such as India and China. These markets grow rapidly and there are several unmet medical needs. With the industry presence, patients will benefit. However, it is of course of extremely important that the operations in these countries are up to acceptable standards. Industry should continue to work closely with the vendors. Both in collaboration to solve issues and improve performance, but also from more strict auditing protocols. For instance, during 2009, Pfizer conducted more than 100 environmental audits on third party manufacturers. You can read about Pfizer EHS External Supply program via this link. Read also this stakeholder commentary from Pfizer’s 2009 Corporate Responsibility Report regarding our work with our 3rd party manufacturers. Mr Ramaprasad Reddy (Chairman at Aurobindo which is the vendor being discussed under item Ekot 6 above) says the following:

“Corporate responsibility at Pfizer must be the work of every department on every day, and is what has attracted Aurobindo most as being one of the latest entrants into the Pfizer family of stakeholders. Pfizer has not only selected us as one of the stakeholders this year, but really proved it to us by collaborating and working with our teams in supply chain. Pfizer performed an audit to determine supply chain capability, and diagnosed certain deficiencies giving us 2.5 points on a scale of 4 and suggested Advanced Planning Scheduling (APS) and Vendor Management Interface. These inputs have been taken very positively by Aurobindo and are now reaping benefits. With the implementation of the above inputs, we should be moving to a 3+ on a scale of 4. Aurobindo is keen to understand “technology and innovation strategy” for manufacturing facilities to reduce costs. Right first time strategy, green purchasing and responsible contracting are the strategies equally innovative. We will certainly look at Pfizer results in the months to come to learn and adopt wherever we can!”

As you probably understand, I think companies such as Pfizer and AstraZeneca take responsibility for their supply chain. We could probably do things even better, and I am convinced that our programs will keep on improving over time. But I also strongly believe that governments need to take their part of the responsibility as well. As pointed out under item Ekot 3 above (”The state saves billions on environmental scandal in India”) the pressure on costs from systems such as the Swedish “generic reform” is also part of the problem, and hence most likely could also be part of the solution. I strongly recommend you to read the article from fall 2010 in Veckans Affärer where the situation in India is discussed in relation to the generic reform.

I like to come back to Richard Bergström’s comment from MiljöRapporten Direkt. It is important that it becomes economically viable to take sustainability initiatives. Then there must be some kind of “green incentives” within the pricing and reimbursement systems and not only a focus on “lowest, lowest, lowest possible price”…

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