プロフィール詳細

プロジェクトを作成

★★★★★

☆☆☆☆☆

★★★★★

☆☆☆☆☆

Neha S.に依頼

India

Freelance Regulatory assistance and medical writing assistance

プロフィール概要

Strongly reliable and focused Regulatory Affairs Specialist with great depth and breadth of experience in medical device regulation and reporting in India. Managed timelines, and handled domestic and international product registration, including renewals. Superb multitasker, is able to handle multiple projects efficiently and accurately. Effective independent worker as well as excellent coordinator with other members of a regulatory affairs team.

専門分野

• ★ Medical Device Regulatory Consulting
• ★ Regulatory Writing
• ☆ Telecommunications
• ☆ Wireless Communication

サービス

• Writing
• Research
• Consulting
• Product Development

Writing Clinical Trial Documentation, Medical Writing, Non-Medical Regulatory Writing, Technical Writing

Research Market Research, User Research, Feasibility Study, Gap Analysis, Gray Literature Search, Systematic Literature Review, Secondary Data Collection

Consulting Digital Strategy Consulting, Scientific and Technical Consulting, Regulatory Consulting

Product Development Product Evaluation

職務経験

Consultant PV

ClinChoice

8月 2022 - 現在

Regulatory Affairs (Drugs, Cosmetics and Medical Device)

Freelancer

11月 2017 - 現在

Regulatory Specialist

Apcer Life Sciences

1月 2017 - 11月 2017

REGULATORY ASSOCIATE

Stryker Global Technology Center

5月 2016 - 12月 2016

Project coordinator

PPD India

5月 2015 - 1月 2016

Clinical Coordinator

Tech-Observer India Pvt Ltd.

9月 2012 - 9月 2014

学歴

Master in pharmacology

RKDF University Bhopal

10月 2014 - 1月 2017

認定資格

• Technical Writing

  IIIM SKILLS

  1月 2022 - 現在

• Business Communication

  Internshala

  1月 2020 - 現在

• Post Graduate Diploma in Clinical Research and Pharmacovigilance

  Clinimind India

  8月 2011 - 現在