Report from Europe - Pharmaceutical Technology

Latest Issue

Latest Issue
PharmTech Europe

Report from Europe
The European Commission and Medicines Agency seem to be moving in advance of their ICH partners to update standards.

Pharmaceutical Technology
Volume 35, Issue 1, pp. 18, 20

Because the ICH guidelines cover individual aspects of pharmaceutical manufacture, there is no uniform single ICH guideline for GMP for finished products, according to EMA. That said, "....there is pre-existing broad equivalence in requirements," says the EMA spokesperson. "We are in regular contact with our US and Japanese colleagues under different frameworks and do not believe that the changes proposed are inconsistent with existing or planned requirements of those international partners."

Nonetheless, the divergences are beginning to concern manufacturers of medicines and APIs. "In general, we always advocate that requirements should be harmonized between geographic areas as much as possible," says Chris Oldenhof, president of the Active Pharmaceutical Ingredients Committee (APIC), a branch of the European Chemical Industry Council.

API producers in Europe are also worried that the scope of the alterations on starting materials could be too broad to be effective. "If the required changes are to apply further upstream to include raw and starting materials throughout the synthesis chain then they will not be realistic," says Oldenhof, who is also manager of external regulatory affairs at DSM (Heerlen, The Netherlands). "It is well-known that unrealistic requirements usually lead to widespread noncompliance and even fraud."

The European Commission has declined to amend the EU guideline to allow for mandatory GMP inspections by regulatory agencies of API plants, which has been a long-established demand of European API producers. "Without adequate plant inspections, levels of compliance will always be quite low," says Oldenhof. "This is the main weakness of the proposals."

For APIC and the European Fine Chemicals Group, which also represents API producers, the Commission's suggested changes are welcome overall because they tighten up existing GMP controls in an area in which it is notoriously difficult to enforce regulations.

Sean Milmo is a freelance writer based in Essex, UK.


blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
| Weekly

Which of the following business challenge poses the greatest threat to your company?
Building a sustainable pipeline of products
Attracting a skilled workforce
Obtaining/maintaining adequate financing
Regulatory compliance
Building a sustainable pipeline of products
Attracting a skilled workforce
Obtaining/maintaining adequate financing
Regulatory compliance
View Results
Eric Langer Outsourcing Outlook Eric LangerBiopharma Outsourcing Activities Update
Cynthia Challener, PhD Ingredients Insider Cynthia Challener, PhDAppropriate Process Design Critical for Commercial Manufacture of Highly Potent APIs
Jill Wechsler Regulatory Watch Jill Wechsler FDA and Manufacturers Seek a More Secure Drug Supply Chain
Sean Milmo European Regulatory WatchSean MilmoQuality by Design?Bridging the Gap between Concept and Implementation
Report: Pfizer Makes $101 Billion Offer to AstraZeneca
Medicare Payment Data Raises Questions About Drug Costs
FDA Wants You!
A New Strategy to Tackle Antibiotic Resistance
Drug-Diagnostic Development Stymied by Payer Concerns
Source: Pharmaceutical Technology,
Click here