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I will write technical documents for medical device submissions iso 13485, sops, ce mdr

S. Komal

Pakistan

I speak English

Regulatory Pharmacist, Business Graduate, Medical and Business Writer

Hi, I’m Shahzeena 👋 A qualified Regulatory Pharmacist with strong expertise in medical and pharmaceutical sciences, pathology, and anatomy. My academic background allows me to approach complex topi...
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About this Gig

Are you looking for professionally written medical device technical documentation that meets regulatory expectations?


I am a Regulatory Affairs professional with hands-on experience in medical device documentation and compliance. I can help you prepare clear, accurate, and well-structured regulatory documents for manufacturers, importers, distributors, and startups.


My services include:


* Technical File documentation

* Device Description

* Intended Use

* Essential Principles / GSPR documentation

* Labeling and IFU review

* Declaration of Conformity (DoC)

* Regulatory letters and supporting documents

* Document formatting and proofreading

* Compliance document review


Why choose me?


️ Regulatory Affairs experience in the medical device industry

️ Professional, confidential, and accurate documentation

️ Timely delivery

️ Revisions based on your requirements


Please contact me before placing an order so we can discuss your device, regulatory market, and documentation requirements.

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write technical documents for medical device submissions iso 13485, sops, ce mdr

Document type:

Standard Operating Procedures (SOPs)

+1 more

Industry:

Medical & biotech

Language:

English

Delivery style preference

Please inform the freelancer of any preferences or concerns regarding the use of AI tools in the completion and/or delivery of your order.

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