プロフィール詳細

プロジェクトを作成

★★★★★

☆☆☆☆☆

★★★★★

☆☆☆☆☆

Sonali S.に依頼

India

8yr of Experience in EUMDR | 510k submission | Risk management ISO 14971 | ISO 13485 | MDSAP | Post Market Surveillance

プロフィール概要

8yr of Experience in EUMDR | 510k submission | Risk management ISO 14971 | ISO 13485 | MDSAP | Post Market Surveillance

専門分野

• ☆ Medical Devices
• ☆ Post-Market Surveillance
• ☆ Medical Device Regulatory Consulting
• ☆ European Medical Device Regulation (MDR)
• ☆ ISO 13485
• ☆ ISO 14971
• ☆ Clinical Trials
• ☆ Regulatory Affairs
• ☆ Risk Management

サービス

• Writing
• Research
• Consulting
• Data & AI
• Product Development

Writing Medical Writing, Non-Medical Regulatory Writing, Technical Writing

Research Market Research, User Research, Meta-Research, Gray Literature Search

Consulting Scientific and Technical Consulting, Regulatory Consulting

Data & AI Statistical Analysis

Product Development Stability/Shelf Life Testing, Concept Development

職務経験

Freelancer

Freelancer

1月 2018 - 現在

学歴

Bachelor of Pharmacy (Gold Medallist)

Parul university

1月 2014 - 1月 2018

認定資格

• PGDRA

  Global Institute of Regulatory Affairs

  1月 2020 - 現在