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Consensus Document On Biosimilar Medicines Paper Is Now Available In Five Languages

Brussels, 25 June 2014 – After its successful launch in May 2013, the European Consensus Information Paper What you need to know about Biosimilar Medicinal Products is now available in English, French, German, Italian, Spanish and later this summer, Portuguese.

This important comprehensive paper is a result of a co-operation of all relevant European stakeholders. It provides a clear and unbiased view of biosimilar medicines and how they are contributing to healthcare in Europe. It was elaborated in the context of the European Commission’s Process on Corporate Responsibility in the Field of Pharmaceuticals and specifically the platform “Access to Medicines in Europe”, which focused on a number of topics including biosimilar medicines.

This collaboration has since continued in order to make this multi-stakeholder paper accessible for patients, healthcare professionals, scientific societies and competent authorities in more languages. The involvement of industry, patient representatives, clinicians and national payers and the Commission ensured that these translations remain faithful to the original document.

The Consensus Information Paper What you need to know about Biosimilar Medicinal Products is available in English, French, German, Italian and Spanish here, together with the other deliverables of the Project Group on Market Access and Uptake of Biosimilars.

Source: EGA Press release

Falsified / stolen pharmaceutical products circulate in Germany!

German authorities are investigating currently the incidence of falsified / stolen Biopharmaceutical products originating from Italy. According to a BKA spokesperson six products are under scrutiny – Avastin, Mabthera, Herceptin, Remicade, Alimta and Humatrope.

End of April EMA already warned about falsified Herceptin circulating on the german market. Obviously the Herceptin was stolen from italian hospitals and were sold via a UK wholesaler to german PI companies. The concerned batches were recalled from the german market.

Rumor has it that 2 truckloads were stolen from Roche in Italy during transportation last December. Why the concerned batches were not recalled instantly is not known yet. There is a high risk that due to improper transporation temperature the quality of these goods may have been negatively impacted before they may have reentered to supply chain.

On May 29th the warehouse of the pharma-forwarder “trans-o-flex” in Neuss was burgled. The thieves took 53 pharmaceuticals of Eurim Pharm, Johnson & Johnson, McNeil, MSD SHARP & DOHME, Bayer Vital, Janssen Cilag, CC Pharma and others.

The list of stolen articles becomes longer day by day. Actuals List per 12.6.2014 of stolen products and batches can be found here (German only) – click on the red text and a PDF should open – batches are listed page 3 ff.

The German “Arzneimittelkommission” advises to check the incoming goods since May 29th of the affected batches and deeply check them for any hints of manipulation.

Biocad’s biosimilar rituximab receives approval in Russia

The rituximab biosimilar which will be marketed under the trade name AcellBia, is the first mAb biosimilar to receive positive opinion from the Russian regulatory body.

The Russian MoH’s positive opinion on AcellBia is based on the results of randomized multicenter clinical study comparing the pharmacokinetics, pharmacodynamics, safety, and efficacy of BCD-020 (rituximab biosimilar by BIOCAD) to the innovator rituximab. The registration clinical study of rituximab biosimilar in CD20-positive indolent non-Hodgkin’s lymphoma patients started in Russia in the end of 2011, and by mid-2012 it already involved over thirty centers in Russia, Ukraine, India, and South African Republic.

BIOCAD started work on rituximab biosimilar in 2010 in the context of a federal innovative project that was approved by the Presidential Commission on Modernization and Technological Advancement. The scope of the project included in-house development of mAb manufacturing technology, comprehensive characterization of developed biosimilars, comparative non-clinical and clinical studies.

The approval of AcellBia is definitely good news for patients who previously had limited access to advanced therapeutics, and in particular for those hindered by the extra high cost of antibody biopharmaceuticals. BIOCAD’s founder expressed hope that domestic capacity for production of high-quality, high-value biosimilars for treating diseases with the most profound social impacts will not only make the drugs more affordable, but will also help make the Russian healthcare sector less dependent on foreign imports.

BIOCAD’s rituximab biosimilar is produced in a special economic development district outside of St. Petersburg. BIOCAD is also finishing clinical trials of two more mAb biosimilars, bevacizumab and trastuzumab (biosimilars of Herceptin and Avastin by Hoffmann-La Roche), that will be produced at the same facility. The company has ten more mAb-based biosimilar and original products in the pipeline.

Source: BIOCAD press release


GMDP Database showing Certificates, Licenses and Non-Compliance.
EudraGMP is the database of the European Community of manufacturing authorisations and of certificates of good manufacturing practice. The EudraGMP system was launched in April 2007, for use by European Medicines Regulators. General public access  via Internet is available since 2009.

Information can be found about:
MIA – Manufacturing and import authorizations
GMP – Good Manufacturing Practice (GMP) certificates.
GMP – Statements of non-compliance with GMP

EudraGMDP – D is the new part regarding DISTRIBUTION – is the new name for the Union
database since 2013.

In addition the following new information are available:
WDA –  Wholesale Distribution Authorizations
GDP – Good Distribution Certificates
GDP – Statements of non-compliance with GDP
API –  Registration of manufacturers, importers and distributors of active substances for human use
located in the EEA

All GMP and GDP certificates are listed in a database by the European Medicine Agency and all GMP and GDP authorities in Europe should enter the GMP and GDP certificates via an interface into this  EMA database.

It’s not complete yet, but it’s growing:

Nearly 700 GDP certificates have been recently added in the EudraGMDP, and also two GDP-non-compliance-reports have been published yet –  on 19.02.2014 + 27.03.2014 , both by the Czech authority.

There the important information wghile using that database may not be forgotten: The absence of a GDP/GMP certificate should not be understood as meaning that the active substance manufacturer in question does not comply with GDP/GMP.


Germany has not entered any data yet – not one single German WDA or GDP certificate can be found.

Anyhow Medizone is full compliant to GDP ( )

and of course holding a valid WDA (

The database can be accessed via

Also a list of the National Competent Authorities (NCA) of the EEA can be found:


The EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and Medicinal products – quality, safety and efficacy

Has published additional information to the GDP 2013/C 343/01




The documents sets out frequently-asked ‚questions and answers‘ regarding the new

guidelines on Good Distribution Practice of medicinal products for human applicable as

of 8 September 2013, and their revision of November 2013.

It can be found

Medizone and PassionBio agree on closer cooperation

PassionBio’s provides drug development, regulatory and commercial solutions for biologics, biosimilar/-better or mAb programs. Our aim is to foster cross-frontier development of your biosimilar portfolio. We support you with (pre-)clinical trial design and with your interactions with EU regulatory authorities. We help you select the right CRO and negotiate competitive budgets with CROs and other contractors in Europe. For more information please refer to our corporate site on PassionBio LinkedIn  or visit

New EU GDP Guidelines – Part II

The “Guidelines on Good Distribution Practice of Medicinal Products for Human Use” have been published 07.03.2013. But only a few months later the GDP had to be renewed. The new version 2013/C 343/01 “corrects factual mistakes identified in subchapters 5.5 and 6.3 of the revised guidelines. It also gives more explanations on the rationale for the revision as well as a date of coming into operation.” (1)

Medizone happily acknowledged, that many of the additional translations errors were corrected by establishing the German translation of 2013/C 343/01.

Unfortunately there again are some new translation mistakes in the German GDP of 05.11.2013, but less than before.
This might be subject to another news coming up soon.

Medizone is up2date and full compliant also to the newest version of the Guidelines. These are some more of the action items we performed and the results, we achieved:

  • 100% of transportation with qualified and audited logistics partners
  • Stringent rules on transport and temperature monitoring during transport work well, proven by self-inspection in February 2014.
  • Risk-Based self-inspection-plan has been implemented.
  • Risk-Based process on temperature control has been established and shows success while testing it in real life.
  • All SOP’s have been again reviewed to ensure full compliance to the newest Version of the Guidelines of November 2013.
  • Description of the computerised systems of Medizone Germany GmbH as requested by GDP 2013/C 343/01 of 05.11.2013 has been finalized.

To be continued…

(1) Introduction Section 3

With our procedures we try to get even better day by day to provide better service to our clients.

MabThera SC now approved in EU for patients with non-Hodgkin lymphoma

Roche announced today that the EU Committee for Medicinal Products for Human Use (CHMP) recommended that the European Commission approve MabThera (rituximab) 1400mg solution for subcutaneous (SC) injection for the treatment of patients with common forms of non-Hodgkin lymphoma (NHL).

“We are excited the MabThera SC data confirm the efficacy and safety of a significantly shortened treatment time,“ said Sandra Horning, M.D., Chief Medical Officer and Head, Global Product Development. “We are confident that reducing treatment to approximately five minutes with MabThera SC will be an improvement for patients and healthcare professionals alike.”

Currently, MabThera is delivered by an intravenous infusion which takes approximately 2.5 hours. The new MabThera SC formulation can be delivered over approximately five minutes and comes as a ready-to-use, fixed dose, which reduces pharmacy preparation time and overall impact on hospital resources.

The CHMP opinion is based primarily on data from the phase III SABRINA study. Roche expects a final decision from the European Commission in the coming months.

Source: Roche press release


Medizone supports “Wings for Life” Foundation

The driving forces behind Wings for Life are the two-time motocross world champion Heinz Kinigadner and the founder of Red Bull, Dietrich Mateschitz. In 2003, Kinigadner’s son Hannes had a tragic accident at the age of 19 which left him tetraplegic.

Moved by the dreadful injury, Kinigadner and Mateschitz invited leading scientists from across the world to come to Salzburg. It soon became clear that, contrary to common opinion, there is legitimate reason to hope that traumatic spinal cord injury can be cured. Ground-breaking discoveries made by Prof. Dr. Sam David in 1981 and by Prof. Dr. Martin Schwab in the early 1990s showed that injured nerve cells in the spinal cord are capable of regeneration after specific types of treatment.

Kinigadner and Mateschitz soon realised that research into spinal cord injury was underfunded. Paralysis is not considered a widespread condition and therefore investing millions in research to help a relatively small number of people was generally considered an unprofitable endeavour.

This realisation prompted Kinigadner and Mateschitz to set up the Wings for Life research foundation – with the goal of finding ways to cure all people affected.

100% of donations are used to fund basic research as well as preclicincal and clinical studies of promising new therapies and drugs. The administration costs are borne entirely by Red Bull.


„My grandfather spent more than half of his life in a wheel chair after an accident. A friend of my son is paralyzed since years after a ski accident. It can happen to anyone of us. The question is not whether effective treatments and cures will be found, but when they will be found!
We are proud to support Wings for Life!“

Gerhard Hoerl
Managing Director – Medizone Germany

Biocon-Mylan’s Biosimilar of Herceptin approved in India

Biocon, India’s largest listed biotechnology company, informed it had received marketing authorisation from the Drugs Controller General of India (DCGI) for its trastuzumab biosimilar, being developed jointly with US’ Mylan, for the treatment of HER2+ metastatic breast cancer. The product will be launched during the last quarter of this financial year.

This is the first approval for a biosimilar product developed by Biocon and Mylan, which joined the project in 2009. The product is a biosimilar to Swiss pharma giant Roche’s Herceptin, used for the treatment of this type of breast cancer. Biocon and Mylan will sell products under CANMAb and Hertraz brand, respectively. Biosimilars are independently developed follow-on versions of medicines after their patent has expired.