More Flexibility in Sterility Testing of biologic Products – FDA Amendments
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On January 2011, the presidential document Executive Order 13563 for “ Improving Regulation and Regulatory Review“ was published in the Federal Register Vol.76, No.4.. This order comprised requirements like “Our regulatory system must protect public health, welfare, safety, and our environment while promoting economic growth, innovation, competitiveness, and job creation. It must be based on the best available science“ or „It must identify and use the best, most innovative, and least burdensome tools for achieving regulatory ends“.
In response to that order and to keep pace with scientific advances, the FDA published “Amendments to Sterility Test Requirements for Biological Products”. This document is supposed to provide manufacturers of biological products with greater flexibility, as appropriate, and encourages the use of the most appropriate and state-of-the-art test methods for assuring the safety of biological products.
Following the Summary of that Final Rule it
eliminates specified sterility test methods, culture media formulae (or formulation), and culture media test requirements;
eliminates specified membrane filtration procedure requirements for certain products;
eliminates specified sterility test requirements for most bulk material;
modifies the repeat sterility test requirements, so that repeat tests will occur only once for each lot. These repeat tests are limited to situations when the quality control unit conclusively determines, after conducting an investigation upon detection of viable microbial contamination during the initial test of the lot, that the contamination is the result of laboratory error or faulty materials used in conducting the sterility test;
replaces the storage and maintenance requirements for cultures of test organisms used to determine the “growth-promoting qualities” of culture media with: (1) Validation requirements specifying that any sterility test used is able to consistently detect the presence of viable contaminating microorganisms and (2) verification of “growth-promoting properties” or microorganism-detection capabilities of test and test components;
replaces the sample size or amount requirement with a requirement that the sample be appropriate to the material being tested;
replaces the Interpretation of test results section under § 610.12(c) with a requirement that manufacturers establish, implement, and follow written procedures for sterility testing that describe, at a minimum, the test method used, the method of sampling, and the written specifications for acceptance or rejection of each lot;
simplifies and clarifies the Exceptions section under § 610.12(h);
identifies the Director of CDER as one of the two Center directors authorized to grant an exemption under the exception provision at § 610.12(h)(2). In the proposed rule, the Center for Devices and Radiological Health was erroneously identified in this exception, instead of the Center for Drug Evaluation and Research.
revises the definition of the term “sterility” under § 600.3(q);
eliminates certain exceptions for allergenic products related to sterility testing under § 680.3(c).