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Clarity

Rosemary Omlin

Background in the medical device / drug industries with experience setting up Quality Management Systems. Extensive background in managing of contract manufacturers, auditing of contact manufacturers, CROs and contract testing labs. An ISO 13485 Lead Auditor

$3.33/min

5 Calls

1 Review

17 minutes
Avg. call

Drug Development FDA Medical Device R&D Regulatory Compliance

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FDA Medical Device/Drug Expert

Background in the medical device / drug industries with experience setting up Quality Management Systems. Extensive background in managing of contract manufacturers, auditing of contact manufacturers and contract testing labs. An ISO 13485 Lead Auditor

Answers 0
Reviews 1

Answers

Reviews

Rosemary provided me with some clear answers to my queries and give me some areas to investigate further. Appreciated the candour about areas beyond her expertise. Hours of research eliminated thanks to a 15-minute call – brilliant. Thank you, Rosemary.

Keith Mander Source: Clarity

Member since August 2017