Tuesday, August 19, 2008

BECOME A FREE LANCER REGULATORY AFFAIRS CONSULTANT

Regulatory Affairs is a great and ever increasing career which happened to be in pharmaceutical industry and the profession is most rewarding and lucrative.The profession creates numerous opportunities not only as a regulatory professional in industry but also a freelancer consultant.

Who is a Freelancer regulatory consultant ?

A freelancer regulatory consultant works for national and offshore pharmaceutical company or sometimes they have to work for a short period with their In-house regulatory team.

Freelancer regulatory consultants need to contact medical and regulatory agencies for early approvals and prepare documents showing efficacy and safety of indications as a part of their work

What are the Possibilities for career in future ?

To become a regulatory consultant one should have sound knowledge background and above all should be well versed with the regulatory environment and regulatory skills.One can start his/her career as a regulatory consultant business.

Important skills for someone to become a regulatory consultants ?
One should have critical ability to translate intricate terms and content into more simpler and precise manner which is easier to understand.

One can convince assessors and their clients that you have a right approach and views.

One should have regulatory skills while contacting and meeting healthcare regulatory agencies.

Go for it! Ways of working for Pharmaceuticals varies from industry to industry and Scope of opportunities in this sector are great.
For Careers And Job Oppurtunities In Regulatory Affairs Read More Updates And Relevant News On Blog



23 comments:

Anonymous said...

Hi!!!!!!!! Myself a regulatory professional. planning to start my rgulatory consultancy but not able to head to the appropriate path. please help me out in doing this. mail me on this topic on my email id siddhisohani@yahoo.co.in

Fda Regulatory Affairs said...

Thanks for this great post........

SKblog said...

Hi, thanks for this post. Iam Shilpa and in the RA profession for almost a decade and covered most of the international countries. I have worked as a freelancer for few indian companies and now looking to start my own freelancing regulatory affairs. If anyone's interested pl do contact me on +91 9892291183 or on my email: shilpa_bangera@yahoo.com.

Unknown said...

Hi, I am Suresh, worked for several years in Regulatory Affairs in Pharmaceuticals/ Biologicals. Let me know if any of you would like to seek any advices and use my expertise. I can be contacted +91 9701054069 and write e-mail at grechemlabs [at] gmail [dot] com.

Anonymous said...

Hi I am shelly koshal. I have an experience of about 9 years in regulatory affirs ( Medical Device and Pharmaceiticals) for the Indian market. Curently I am interested in looking for free lancer oppurtunities. Please let me know if you seek to use my expertise in regulatory affairs for the medical devices or cosmetics.....

Anonymous said...

Hi
I am sonam jain (M.Pharm Regulatory affairs) having 2 years of work exp in the field of Regulatory Toxicology seeking opportunity to work as freelancer. Kindly help me if anybody come across any such opportunity especially in the field of Cosmetics regulatory affairs. My Email ID is shanushan13niper@gmail.com

Regulatory Support said...

Hello,

We are providing regulatory support with accuracy in documents at very nominal charges for CIS, ROW & european market.

Please contact on below mentioned email address for further details.

formulation.regulatory@gmail.com

Thanks & Regards
Regulatory Team.

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anjali said...

My self Ankita Rathod a pharmaceutical consultant. I offer wide range of services in the domain of product development, regulatory affairs, IPR , Clinical, non clinical , Artwork Development.
I have professionals, domain experts with varied specialization,best suited to meet your requirements at surprisingly low costs.
Please respond with your requirements so that I can respond accordingly.
Key Services Offered :
1. Dossier compilation (CTD, ACTD, DMF, and other dossier as per National guideline), have more than 200 ready original Vendor DMF
2. Analytical method validation, Dissolution Profile
3. Expert report-Quality, Clinical and Non-clinical
4. Prepare Summary of product (SmPC) and Pack Information Leaflet (PIL)
5. Prepare label and carton contents
6. Bioavailability / Bioequivalence / Clinical Trial Studies from approved lab
Please contact to below address for further details
4344nkt@gmail.com /9757396714

Unknown said...

Hi I am Aarti having about 10 yeras of Regulatory experience.. Looking for a freelance Regulatory opportunity..
You may contact me on aarti1chindarkar@yahoo.CO.in

Unknown said...

Hi I am Aarti having about 10 yeras of Regulatory experience.. Looking for a freelance Regulatory opportunity..
You may contact me on aarti1chindarkar@yahoo.CO.in

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Unknown said...
This comment has been removed by the author.
Unknown said...

Its an Excellent Blog on Regulatory Affairs, Blog is most leading and helpful as a career guide which can be rewarded in a pharmaceutical company's as a Free Lancer Regulatory Affairs. For best consultants I recommend
http://www.labeladossier.com/dossier-services.htm. The Medical services and products are amazing and company is best in Regulatory Consultants.

Stratycon said...
This comment has been removed by the author.
Stratycon said...

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Anonymous said...

Hi I am Raj here and having 16 years of total experienc, 11 years in Regulatory Affairs- Regulated market. Now I am interested to start regulatory consultancy of my own. Please guide me how to go about this. Please email me at shvaishu_shetty@rediffmail.com or call me at 9820207225

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