cgmp Latest News

GPMG, a medical device consulting firm, unveiled a quality system product designed for specification developers. The FDA QSR and ISO 13485 compliant system governs all aspects of product development, design transfer, and device master records.

Learn Good Manufacturing Practice (GMP) at International Conference on QA, QC and Validation December 3-5 Philadelphia, PA. Applicable to all industries focused on product quality, especially medical devices. Hands-on Training with industry expert.

ComplianceOnline, the leading GRC advisory network, and leading quality systems advisor Dr. Richard Poser, will conduct a two day, in-person seminar on how to prepare for laboratory inspections and avoid Form 483 observations.

EMSL Analytical’s cGMP and ISO 17025 compliant laboratory provides bioburden and sterility testing for personal care products.

Learn about FDA QSR, cGMP, GMP. How FDA guidelines apply to medical device manufacturing and product quality. Identify gaps in the quality system. Immediately apply learnings in your workplace. Hands on, live instructor training in Miami / Doral.

EMSL Analytical offers FDA-registered lab offers cGMP and ISO 17025 compliant materials testing for pharmaceuticals.

EMSL Analytical provides a wide range of cGMP personal care product testing, including bacterial analysis

EMSL Analytical offers advanced pharmaceutical testing services in our FDA registered and ISO 17025 compliant laboratory

EMSL Analytical offers advanced pharmaceutical testing services in our cGMP and ISO 17025 compliant laboratory

This 6 hour webinar on Pharmaceutical Stability will include a detailed overview of regulatory requirements for Stability Programs, how to design one and report the data in regulatory filings and supporting cGMP systems for a Stability Program.

This seminar will begin by covering a short history of the lyophilization process, the equipment used, types of samples that can and cannot be freeze-dried.

Neuland Labs Joins Leading International Trade Group to Help Support Global Expansion of API and Contract Manufacturing Business

Vizag, India (September 2010) – PharmaZell GmbH, a European Contract Manufacturing Organization for active pharmaceutical ingredients and advanced intermediates, has once again expanded its manufacturing capabilities in India.

As a company going through significant growth, Lawler Foods recognized its need for an ERP that could manage its business and production demands, as well as maintain product quality.

Modern Concepts, Inc. needed an integrated ERP system to track lots, meet ISO9000 reporting requirements, and produce Material Safety Data Sheets - and chose ProcessPro ERP.

Critical information that dietary supplement manufacturers must know in order to meet the FDA's good manufacturing practices “compliance paradigm” is presented in a free white paper, “Dietary Supplements — A New Paradigm for Manufacturers.”

Polysaccharide and Pirkle-type Columns Proved Useful for Numerous Methods

ProcessPro ERP system is a very specific tool designed to meet the high quality standards set at Red Monkey Foods.

Regis Technologies, Inc., announced today that it has expanded its scientific staff with the addition of four scientists formerly employed by deCODE genetics Inc.

St. Cloud, Minn., April 30, 2009 -- ProcessPro, developers of ProcessPro® ERP software, announces the release of its latest version, Premier 10.

Ensur Document Control Software user Daniel Perry of Telegistics, a New Zealand company, is raising funds to support research for cures and treatments of leukemia. He is participating in Shave 2008 of New Zealand.

Deacom, Inc. announces it has joined the Generic Pharmaceutical Association (GPhA) as an Associate Member.