Friday, 13 February 2015

First stem-cell therapy recommended for approval in EU

The European Medicines Agency (EMA) has recommended Holoclar, the first advanced therapy medicinal product (ATMP) containing stem cells, for approval in the European Union (EU). Holoclar is a treatment for moderate to severe limbal stem cell deficiency (LSCD) due to physical or chemical burns to the eye(s) in adults. It is the first medicine recommended for LSCD, a rare eye condition that can result in blindness.

For further details see EMA

Posted by Tim Sandle

Thursday, 12 February 2015

Adaptive pathways for drug development

Adaptive pathways should be the preferred approach in the near future to bring new medicines to patients according to the European Medicines Agency (EMA).

This has been outlined in an article published in Clinical Pharmacology and Therapeutics. The concept of adaptive pathways foresees an early approval of a medicine for a restricted patient population based on small initial clinical studies.

The first approval is followed by progressive adaptations of the marketing authorisation to expand access to the medicine to broader patient populations based on data gathered from its use and additional studies.

EMA launched a pilot project on adaptive pathways (formerly known as adaptive licensing) in March 2014 to explore this approach with real medicines in development.

As of November 2014, the Agency had received and assessed 29 applications as part of the pilot, nine of which had been selected for discussion with the applicant.

For further details, see EMA

Posted by Tim Sandle

Wednesday, 11 February 2015

Mitigating risks due to the use of antibiotics in animals

The European Medicines Agency (EMA) has published recommendations to limit the development of antimicrobial resistance (AMR) linked to the use of antibiotics in animals, thereby minimising at source the risk of transmission of resistance from animals to humans. The document reference is EMA/787672/2014.

The proposed measures focus in particular on promoting the responsible use in veterinary medicine of antibiotics that are critically important in human medicine such as fluoroquinolones and third and fourth generation cephalosporins.

For details see: EMA

Posted by Tim Sandle

Tuesday, 10 February 2015

Pharmacopeial Forum 40 (6)


The USP Pharmacopeial Forum has a new update. This is Volume 40, No.6. Of interest in the new issue is:

General Chapter                                       

Chapter 790   Visible Particulates in injections (Revision proposal target, USP39-NF34)

The chapter has been edited to clarify intent, which is the need to control and have acceptance criteria for extraneous particles, even for drug products that contain inherent particles.

Chapter 851   Spectrophotometry and Light Scattering (Revision proposal target, USP39-NF34)

This general chapter is being replaced by a new series of chapters. The new chapters are:

Chapter 852 Atomic Absorption Spectroscopy
Chapter 853 Fluorescence Spectroscopy
Chapter 854 Mid-Infrared Spectroscopy
Chapter 855 Nephelometry, Turbidimetry, and Visual Comparison
Chapter 857 Ultraviolet-Visible Spectroscopy

Chapter 855 Nephelometry, Turbidimetry, and Visual Comparison [NEW] (Revision proposal target, USP39-NF34)

A replacement chapter for <851>Spectrophotometry and Light Scattering. The majority of text in this new chapter is the same as <851>.

Chapter 1251 Weighing On An Analytical Balance (Revision proposal target, USP39-NF34)

Additional changes are being introduced in order to align with recent modifications introduced in Chapter 41 Balances.

Posted by Tim Sandle

Monday, 9 February 2015

Industrial Pharmaceutical Microbiology: Standards & Controls (2015)

A new edition of the essential microbiology book “Industrial Pharmaceutical Microbiology: Standards & Controls” has been published.

This publication covers the entire spectrum of industrial pharmaceutical microbiology, as applicable to pharmaceuticals and healthcare and it has been edited by Professor Geoff Hanlon and Dr. Tim Sandle.

The contamination control of pharmaceutical and healthcare environments and processes, together with pre-clinical drug development labs, requires a far more holistic approach than simply choosing technologies and disinfectants. Today the microbiologist is expected to understand industrial processes and cleanrooms, and how to effectively evaluate microbial risks to products from personnel and processes.


To meet the latest regulatory expectations, the role of the microbiologist is essential. In addition there is important input requirement from quality assurance personnel, engineers, and process specialists. Whilst there is a continuing need for monitoring of the environment and conducting standardised laboratory tests, industrial pharmaceutical microbiology has moved on a great deal in the past decade. It now has to embrace microbiological audits; rapid microbiological methods; conducting risk assessments, both proactive in terms of minimising contamination, and reactive in terms of addressing microbial data deviations; and also ensuring that processes meet ‘quality by design’ principles. In this new 600 page book a team of 24 international authorities will assist you in all your questions.

Industrial Pharmaceutical Microbiology: Standards and Controls covers the entire spectrum of industrial pharmaceutical microbiology, as applicable to pharmaceuticals and healthcare. Connect instantly with regulations and current best practices on everything from disinfectants to sterility testing; environmental monitoring to hazard analysis; and from pharmaceutical processes to biological indicators. All of this is developed from an international perspective, where different regulations are compared and contrasted together with insightful commentary as to best practices.

Industrial Pharmaceutical Microbiology: Standards and Controls provides clear, practical and up-to-date guidance for handling virtually every compliance and operational challenge associated with pharmaceutical microbiology.

For details and to order a copy, see: Euromed

The chapter list is:

Part A: The Role of the Microbiologist and the Microbiology Laboratory

1. Safety in Microbiology
Nigel Silman and John V Daniels

2. Best Practices in Microbiology Laboratory Training
Tim Sandle

3. The Use of Culture Media in Pharmaceutical Microbiology
Tim Sandle

4. Rapid Microbiological Methods and Process Analytical Technology (PAT)
Jeanne Moldenhauer

5. Microbial Risk Assessments for Operational Cleanrooms
Tim Eaton

6. The Role of the Qualified Person in Microbiological Quality Assurance
John Dolman

7. Auditing the Pharmaceutical Microbiology Department
Andy Martin

Part B: Microbiological Control and Industrial Processes

8. Microbiological Environmental Monitoring
Rosamund M Baird

9. Selection and Use of Cleaning and Disinfection Agents in Pharmaceutical Manufacturing
Tim Sandle

10 Microbiology of Pharmaceutical Grade Water
Tim Sandle

11. Biofilm Contamination in Pharmaceutical Facilities
Alex P Blanchard

12. Cleanrooms, Isolators and RABS: Basic Principles, Design, Testing, Operation and Regulatory Aspects
John Neiger

13. Aseptic Process Simulations/Media Fills
Marco Budini and Francesco Boschi

14. Filtration
Claire Jarmey-Swan

15. Sterilisation Technologies
Eric Dewhurst and Eamonn Hoxey

16. Biological Indicators
Tim Sandle

17. Endotoxins and Dehydrogenation
Karen Zinc McCullough

18. Containment System Integrity: Microbial Challenges for Sterile Products
Tim Sandle

19. Challenges of Bacteriophage Therapy
Alexander Sulakvelidze

Part C: Regulatory Aspects of Industrial Pharmaceutical Microbiology

20. Microbiological Quality and Regulatory Requirements for Biotherapeutics
Daniel Galbraith

21. The Microbiological Quality and Regulatory Requirements for Natural and Nutraceutical Products
Martin Dennison

22. The Regulatory Control and Quality Assurance of Immunological products
Tim Sandle

23. Regulatory Guidelines (Microbiology) for Veterinary Medicinal Antimicrobial Products
Klaus Hellmann and Peter Silley

24. Regulatory Expectations for Non-Sterile Manufacture of Pharmaceutical Dose Forms
Edel Fitzmaurice

25. The Pharmacopoeias and Microbiology
V Fenton-May

For details and to order a copy, see: Euromed

Posted by Tim Sandle

Gerpac pharmacy meeting review


Nearly 500 delegates gathered at the GERPAC conference in Hyères in France todiscuss aspects of aseptic preparation including cytotoxic contamination in theworkplace and home, risk assessment, disinfection and syringe integrity testing.

"Tim Sandle (Head of Microbiology, Bio Products Laboratory Ltd, UK) and it is important to understand the different roles and properties of detergents and disinfectants when managing a clean room."

Hospital Pharmacy Europe have reviewed the conference, the review can be accessed here.

Posted by Tim Sandle

Sunday, 8 February 2015

Safe, effective meningitis A vaccine for infants


The World Health Organization (WHO) has opened the door to routine immunization of infants in sub-Saharan Africa by approving for use an innovative and affordable vaccine that has all but rid the meningitis belt of a major cause of deadly epidemics.

In the four years since its introduction in Africa, MenAfriVac® has had an immediate and dramatic impact in breaking the cycle of meningitis A epidemics, leading the safe, effective technology to be approved by WHO through its prequalification process for use in infants, and paving the way for protecting millions more children at risk of the deadly disease. The announcement was made today by the Meningitis Vaccine Project (MVP)—a partnership between the global health nonprofit PATH and WHO—and Serum Institute of India Ltd (SIIL), which manufactures the MenAfriVac® vaccine.

“Initial mass vaccination campaigns with MenAfriVac® have been highly effective in reducing the number of meningitis A cases,” said Dr. Marie-Pierre Préziosi, director of MVP. “But epidemics will return when rising numbers of unprotected newborns become a larger proportion of the total population over time. Now, with this decision, health officials will be able to ensure that population-wide protection is sustained by routinely immunizing infants.”

The WHO decision means that the new, 5 µg dose of the meningitis A vaccine meets international standards of quality, safety, and efficacy and can therefore be administered to children younger than one year of age in Africa. MenAfriVac® had previously been authorized for use in children and young adults, aged 1-29 years.

Before the introduction of MenAfriVac®, people living in countries of the meningitis belt, which stretches from Senegal in the west to Ethiopia in the east, were regularly struck by meningitis A epidemics in which sudden onset of symptoms could rapidly lead to death or permanent disability. One of the most devastating outbreaks ever recorded was in 1996-1997, when an epidemic wave infected more than 250,000 people and killed over 25,000 in just a few months. The only existing vaccine was insufficient to break the cycle.

In 2004, MVP partnered with SIIL to develop an affordable, tailor-made vaccine for use against meningitis A in sub-Saharan Africa. MenAfriVac® was developed in record time at less than 1 tenth the cost of a typical new vaccine. Since campaigns started in 2010, MenAfriVac® has been administered to over 215 million people in 15 countries of the African meningitis belt: Benin, Burkina Faso, Cameroon, Chad, Côte d’Ivoire, Ethiopia, Ghana, Mali, Niger, Mauritania, Nigeria, Senegal, Sudan, Togo, and The Gambia.

“Developing the MenAfriVac® vaccine fit exactly Serum’s ingrained philosophy of bringing down prices of vaccines so that under-privileged children of the world are protected,” said Dr. Cyrus Poonawalla, CEO of SIIL, headquartered in Pune, India. “We at Serum Institute are extremely proud of being part of an international partnership that brought an end to a public health issue that has been plaguing sub-Saharan Africa for more than a century.”

One year after large-scale vaccine introduction in late 2010, for example, experience from Burkina Faso provided early evidence that mass vaccination was associated with a significantly reduced risk of meningitis in the targeted population, as well as among the unvaccinated age groups, suggesting MenAfriVac® induced “community” protection. Findings were confirmed in a major way in Chad in 2012 where researchers reported a dramatic reduction in transmission and incidence of meningitis A, a drop of more than 90 percent following vaccination.

Support from Gavi, the Vaccine Alliance; the United Nations Children’s Fund (UNICEF); PATH; WHO; and national governments has been crucial for mass vaccination campaigns that are due to continue until 2016 to cover at-risk populations in all 26 countries where disease burden from meningitis A is greatest.

In parallel to the large-scale vaccination campaigns, clinical studies were designed and conducted to determine the safety, immunogenicity, and optimal dosage and immunization schedule for administering MenAfriVac® to infants and toddlers alongside other routine childhood vaccines in African meningitis belt countries.

Results from two infant clinical studies in Ghana and Mali and vaccine introduction impact data were presented to the WHO Strategic Advisory Group of Experts on Immunization (SAGE) in October 2014, and these SAGE experts concluded that a one-dose schedule at 9 months of age or older was recommended to achieve sustainable disease control following the initial mass campaigns in 1-29 year olds.

Specifically, the WHO prequalification that was announced today allows United Nations procurement agencies to purchase the vaccine for use in routine immunization programs in meningitis-belt countries while serving as an endorsement of quality for countries interested in adopting it.

WHO is already working with African countries to ensure a smooth transition from mass campaigns to routine immunization and so ensure sustainable disease control in the region. Seven countries (Burkina Faso, Cameroon, Chad, Ghana, Mali, Niger, and Nigeria) are in line to introduce MenAfriVac® in their routine systems as early as 2015, while mass vaccination campaigns will continue in remaining countries.

Created in June 2001 with the goal of eliminating epidemic meningitis as a public health problem in sub-Saharan Africa, MVP was one of the earliest product development partnerships funded by the Bill & Melinda Gates Foundation. MenAfriVac® was the first vaccine developed outside “traditional pharma,” and the only vaccine developed specifically for people in Africa.

“With MenAfriVac®, we created a revolutionary new model for vaccine development and now we stand on the brink of protecting an entire generation, and those to come, from a devastating disease,” said Dr. Kathy Neuzil, director of Vaccine Access and Delivery at PATH. “Our efforts began with a request by African leaders to address a major health challenge affecting hundreds of millions of people, and in less than a decade, we proved that a safe, effective vaccine could be developed and deployed across multiple countries at a price that was sustainable.”

“The benefits of childhood immunization last a lifetime and the MenAfriVac® vaccine is one of the greatest success stories that shows what partners can accomplish when we commit together to a compelling cause,” said Chris Elias, president of the Global Development program at the Bill & Melinda Gates Foundation. “Prequalification of the MenAfriVac® vaccine for infants clears the way for the routine immunization of every child before his or her first birthday to ensure long-term meningitis control.”

“We are more than halfway through with introducing the vaccine in meningitis-belt countries, and the first introductions have been a stunning success,” said Dr. Jean-Marie Okwo-Bele, director of the WHO Department of Immunization, Vaccines and Biologicals. “But we cannot yet declare a win on meningitis epidemics in sub-Saharan Africa. If we rest on our laurels and don’t finish the job, meningitis epidemics will return in a major way in the years to come. Elimination of meningitis epidemics will require meningitis belt countries’ political commitment to complete the mass campaigns and introduce the vaccine in the Expanded Programme on Immunization. Then and only then will we win the battle against meningitis.”

FDA's Margaret Hamburg Announces She Will Step Down in March 2015


Margaret Hamburg announced on Feb. 5, 2015 that after almost six years in her role as FDA Commissioner, she will step down from the position at the end of March 2015. According to Reuters, Hamburg announced in a note to staff that her time as FDA chief “has been the most rewarding of my career."

Dr. Stephen Ostroff, FDA’s chief scientist, will take the role as acting commissioner until the position is filled. A potential successor to Hamburg, Robert Califf, MD, a cardiologist and researcher from Duke University, was named by FDA to oversee its drug, medical device, and tobacco policy at the end of January 2015.

Under Hamburg, FDA increased inspection stringency of food and drugs originating from overseas, increased patient engagement in the drug development process, and introduced various measures to speed the development and review of new drugs. In addition to improving existing policies, FDA approved 51 new therapies in 2014, the most in almost 20 years. As noted in the press release on Reuters, Hamburg wrote in a blog post on Feb. 4, 2015 that it is “a testament ... to FDA's innovative approaches to help expedite development and review of medical products that target unmet medical needs."

"Commissioner Hamburg, from day one, has been committed to being a champion for patients. She has fostered the growth of science and innovation across the agency and really changed how FDA and industry collaborate,” said Ellen Sigal, founder and chair of Friends of Cancer Research, in the Reuters announcement.

Source:
Reuters

Posted by Tim Sandle

Saturday, 7 February 2015

New understanding of virus vulnerability

A new study has analyzed how genome mutations of RNA viruses tend to be lethal for these infectious agents. It takes very little to make the RNA too messy and bulky to fit into the capsid -- the shell that contains the viral genome -- and by doing so disrupt the reproductive process. Lošdorfer Bochr('382')ichr('269').

To get into the capsid, the "exoskeleton" of viruses, RNA must be well combed and "packed," because otherwise it will not. The packing of RNA is governed by the genome itself. Based on previous research that demonstrated that viral RNA is normally optimized for packing (outside the capsid it is only slightly bigger than the capsid itself).

Researchers have verified what types of genome alterations preserve the optimization and which instead render the RNA too bulky.

For further details see:

Luca Tubiana, Anže Lošdorfer Božič, Cristian Micheletti, Rudolf Podgornik. Synonymous Mutations Reduce Genome Compactness in Icosahedral ssRNA Viruses. Biophysical Journal, 2015; 108 (1): 194 DOI: 10.1016/j.bpj.2014.10.070

 Posted by Tim Sandle

Friday, 6 February 2015

New Pharmacovigilance Legislation

The new EU 15 modules concerning pharmacovigilance are a major departure in terms of the pharmacovigilance conducted over the last 6 years in Europe since the introduction of Vol IXa. New pharmacovigilance legislation changes apply from April 2015..

The requirements for information provided to Competent Authorities and the European Medicines Agency (EMA) about the pharmacovigilance system(s) of marketing authorisation holders (MAHs) change in several ways: 
  • Summary information only concerning the EU qualified person for pharmacovigilance (QPPV) and the location of a pharmacovigilance system master file will be contained in marketing authorisations.
  • Full descriptive information about the pharmacovigilance system will have to be contained in a pharmacovigilance system master file, which should be made available to the National Competent Authorities upon request.
  • Detailed requirements for the pharmacovigilance system master file concern its availability, structure, content and maintenance.
  • The pharmacovigilance system master file will encompass the pharmacovigilance system and may therefore relate to one or more products, and changes to its content will not be automatically notifiable to the Competent Authorities. This differs from the current Detailed Description of the Pharmacovigilance system (DDPS), which will be phased out over the period from July 2012 to 2015.


 Posted by Tim Sandle

Thursday, 5 February 2015

Safe use of sporicides

Since their introduction, liquid sporicides have become one of the products of choice for many biological research and production facilities wherever high-level microbial control is critical. Although they are marketed as low-toxicity products, appropriate care during use is essential to prevent potentially dangerous conditions, exposures, and injuries.

This forms part of an article by Vince McLeod for Laboratory Manager magazine. The article goes onto state:

“The class of liquid sporicidal disinfectants are popular non-bleach disinfectants used for clean rooms and biosafety cabinets. Since their introduction, liquid sporicides have become one of the products of choice for many biological research and production facilities wherever high-level microbial control is critical. These sporicides make up a category of liquid, cold, fast-acting disinfectants/sterilants primarily used on hard, pre-cleaned surfaces. They provide quick and effective microbial control, including the ability to destroy bacterial spores. They are generally regarded as safe to use on stainless steel, glass, plastics, walls, and floors. Most sporicides are available as a ready-to-use premixed solution or a concentrate and can be applied by immersion, spraying, fogging, or wiping. Although they are marketed as low-toxicity products, appropriate care during use is essential to prevent potentially dangerous conditions, exposures, and injuries.”

To read more, see Lab Manager

Posted by Tim Sandle

Wednesday, 4 February 2015

New antibiotic resistance mechanism

There are two main families of bacteria: those that are surrounded by a single membrane (or one outer wall) and those that are surrounded by two membranes (or two outer walls).

Scientists have examined a protein that is found between these two protective walls, known as RcsF. When all is well, this protein is continually sent to the second outer wall. However, if the bacterium is attacked (by an antibiotic, for instance) the machinery that sends RcsF to the outer wall no longer works: instead of being on the second outer wall, RcsF is stuck between the two fortifications (membranes), from where it sends out an alarm signal. This signal prompts the bacterium to trigger defence systems (by sending other back-up proteins) so as to resist the attacking antibiotic.

In this process, the researchers succeeded in discovering how the protein RcsF manages to sound the alarm. In practical terms, when it is stressed, stuck between the two walls, RcsF contacts another protein, IgaA. The interaction between these two proteins raises the alarm.

For further details see:

Seung-Hyun Cho, Joanna Szewczyk, Christina Pesavento, Matylda Zietek, Manuel Banzhaf, Paula Roszczenko, Abir Asmar, Géraldine Laloux, Ann-Kristin Hov, Pauline Leverrier, Charles Van der Henst, Didier Vertommen, Athanasios Typas, Jean-François Collet. Detecting Envelope Stress by Monitoring β-Barrel Assembly. Cell, 2014; 159 (7): 1652 DOI: 10.1016/j.cell.2014.11.045

Posted by Tim Sandle

Tuesday, 3 February 2015

How Vibrio cholera steals DNA

Scientists have uncovered the unconventional way that the cholera bacterium stabs and kills other bacteria to steal their DNA, making it potentially more virulent. This mechanism, known as "horizontal gene transfer," allows the cholera bacterium to become more virulent by absorbing the traits of its prey. The study is published in Science.

Cholera is caused when the bacterium Vibrio cholerae infects the small intestine. The disease is characterized by acute watery diarrhea resulting in severe dehydration.

For further details see:

S. Borgeaud, L. C. Metzger, T. Scrignari, M. Blokesch. The type VI secretion system of Vibrio cholerae fosters horizontal gene transfer. Science, 2015; 347 (6217): 63 DOI: 10.1126/science.1260064

 

Posted by Tim Sandle

Monday, 2 February 2015

Environmental Monitoring: a Comprehensive Handbook

This is volume 7 of the Environmental Monitoring Handbook series. Each volume of this series discusses different aspects of environmental monitoring. The appendix describes the various topics and authors that can be found in volumes 1 through 6 of this series… There is a wealth of useful information that you can use in establishing, maintaining and updating your environmental monitoring program!

Foe details, see PDA

Tim Sandle has contributed a chapter. The chapter reference is:

Sandle, T. (2015) Cleanroom Design. In Moldenhauer, J. (Ed.) Environmental Monitoring: a Comprehensive Handbook, Volume 7, pp3-28



Sunday, 1 February 2015

What types of bacteria are found in hailstones?

Researchers have found a rich diversity of microbial life and chemicals in the ephemeral habitat of a storm cloud, according to a study published in the journal PLOS ONE by Tina Šantl Temkiv and colleagues from Aarhus University, Denmark.

The researchers found that found that storm clouds carried several species of bacteria typically found on plants and almost 3000 different compounds usually found in soil. However, the hailstones had very few soil-associated bacteria or chemicals that would usually occur in plants.

The article reference is:

Tina Šantl-Temkiv, Kai Finster, Thorsten Dittmar, Bjarne Munk Hansen, Runar Thyrhaug, Niels Woetmann Nielsen, Ulrich Gosewinkel Karlson. Hailstones: A Window into the Microbial and Chemical Inventory of a Storm Cloud. PLoS ONE, 2013; 8 (1)

It can be accessed here: PLOS One

Posted by Tim Sandle

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