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Experts in Practical and Value Added Consulting for the Pharmaceutical/Medical Device/OTC/Cosmetic Industries
Expert Validation Consulting, Inc., offers clients a full range of cGMP compliance, quality systems and validation consulting support in areas including: QC/QA procedures, CAPA, Change Control, Investigations, Process and Cleaning Validation, facilities, ancillary systems or utilities, processing and analytical equipment qualifications, analytical method validations; cGMP compliance audits and assessments, FDA mock inspections, application of risk management and technical consulting; training programs; and computer systems validation. These extend to the pharmaceutical, biotech, bulk pharmaceutical chemical, cosmetic, medical device, veterinary, and biologic industries.
Our consultants have unparalleled industry practical expertise, with an average of 20 years’ experience with pharmaceutical manufacturing and quality operations. They work with clients in all areas of regulatory compliance, all over the world, as they are frequent speakers at international conferences on their areas of expertise. They are also members of Editorial Boards for well-known professional publications focused on pharmaceutical operations.
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