• A GLP laboratory seeks ISO 17025 accreditation
• A bulk pharmaceutical manufacturer requires a Type II DMF
• A research laboratory conducts toxicology studies in support of an IND
• A medical device manufacturer needs an ISO 13485 internal audit
• A chemical distributor requires third-party audits of excipient manufacturers

EM2 can develop a quality system based upon a specific regulation or incorporate regulatory elements in existing quality systems.