The Israeli MoH notified Analyst Research Laboratories that it has successfully passed its latest audit and has been rewarded with an extension of its GMP certification.
The Israeli Institute for Standardization and Control of Pharmaceuticals operating under the Israeli MoH, is recognized by the European Commission under the Agreement on Conformity Assessment and Acceptance of Industrial Products (ACAA), thus ensuring mutual recognition from signatory countries to these agreements.
Analyst’s CEO, Dr. Vivi Ziv commented: “First accredited in 2010, Analyst has maintained throughout the years the highest GMP standards in order to provide our clients with accurate and reliable data”.
“Our real reward”, Dr. Ziv added, “is seeing the data generated in our lab incorporated into our clients’ FDA and other regulatory submissions, and the product we developed and validated methods for – reaching the market”.
About Analyst
Analyst Research Laboratories is a GMP, GLP and GCLP accredited, FDA-inspected contract laboratory. The 1,000sqm modern lab specializes in all aspects of analyzing pharmaceuticals, providing a multitude of Analytical & Bioanalytical services to the pharmaceutical, medical cannabis, biotech and medical device industries. Please visit Analyst’s website for further information at www.analyst-labs.com
Contact
Vivi Ziv, PhD
CEO Analyst Research Laboratories
Tel: +972 50 30 30 244
vivi@analyst-labs.com