Profile Summary
ALOKEPARNA C.
I help medical device startups, diagnostic innovators, and digital health companies build robust and compliant documentation aligned with ISO 1...
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Dr. Anushikha D.
I am a dentist and public health professional with a Master's in Public Health from All India Institute of Medical Sciences (AIIMS), Rishik...
Karissa T.
I’m a seasoned Regulatory Affairs Consultant with over 17 years of experience supporting medical device and IVD companies in achieving global c...
Dr. Harriet K.
Regulatory writing and submissions • Regulatory Intelligence and Strategy Development • Toxicology Study Monitoring • Due Diligence and Gap Ana...
Jarrell M.
I am a medical device professional with 25+ years of experience in R&D product development, risk management, and regulatory compliance. Thr...
Irina B.
QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...
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Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.
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You have to approve the deliverables only if quality meets your expectations. If you arn’t happy, we’ll refund your money.
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EU MDR consulting services needed$550.00
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