medwrite.wordpress.com
Medical Device Regulatory Professional | A resource for regulatory professionals and medical writersA resource for regulatory professionals and medical writers
http://medwrite.wordpress.com/
A resource for regulatory professionals and medical writers
http://medwrite.wordpress.com/
TODAY'S RATING
>1,000,000
Date Range
HIGHEST TRAFFIC ON
Thursday
LOAD TIME
0.2 seconds
16x16
32x32
PAGES IN
THIS WEBSITE
12
SSL
EXTERNAL LINKS
0
SITE IP
192.0.78.12
LOAD TIME
0.173 sec
SCORE
6.2
Medical Device Regulatory Professional | A resource for regulatory professionals and medical writers | medwrite.wordpress.com Reviews
https://medwrite.wordpress.com
A resource for regulatory professionals and medical writers
medwrite.wordpress.com
Medical Device Single Audit Program (MDSAP) Pilot | Medical Device Regulatory Professional
https://medwrite.wordpress.com/2014/09/15/medical-device-single-audit-program-mdsap-pilot
I am a Regulatory Professional, with over 5 years of experience in Regulatory Affairs, and and 10 years of experience writing clinical and regulatory documents. I started this blog as a resource for Clinical and Regulatory Submissions. Medical Device Regulatory Professional. 124; Comments RSS. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Join 41 other followers. Medical Device Single Audit Program (MDSAP) Pilot. Posted on September 15, 2014. Internat...
Medical Device Regulatory Professional | A resource for regulatory professionals and medical writers | Page 2
https://medwrite.wordpress.com/page/2
I am a Regulatory Professional, with over 5 years of experience in Regulatory Affairs, and and 10 years of experience writing clinical and regulatory documents. I started this blog as a resource for Clinical and Regulatory Submissions. Medical Device Regulatory Professional. 124; Comments RSS. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Join 41 other followers. FDA Guidance: Evaluation of Sex-Specific Data in Medical Device Clinical Studies. Http:/ ...
IMDRF: “Software as a Medical Device”: Possible Framework for Risk Categorization and Corresponding Considerations | Medical Device Regulatory Professional
https://medwrite.wordpress.com/2014/11/03/imdrf-software-as-a-medical-device-possible-framework-for-risk-categorization-and-corresponding-considerations
I am a Regulatory Professional, with over 5 years of experience in Regulatory Affairs, and and 10 years of experience writing clinical and regulatory documents. I started this blog as a resource for Clinical and Regulatory Submissions. Medical Device Regulatory Professional. 124; Comments RSS. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Join 41 other followers. Posted on November 3, 2014. This introduces new and unique challenges. For example:.
FDA UDI Rule and GUDID Guidance- | Medical Device Regulatory Professional
https://medwrite.wordpress.com/2014/09/12/fda-udi-rule-and-gudid-guidance
I am a Regulatory Professional, with over 5 years of experience in Regulatory Affairs, and and 10 years of experience writing clinical and regulatory documents. I started this blog as a resource for Clinical and Regulatory Submissions. Medical Device Regulatory Professional. 124; Comments RSS. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Join 41 other followers. FDA UDI Rule and GUDID Guidance-. Posted on September 12, 2014. A device identifier (DI),...
Book Review | Medical Device Regulatory Professional
https://medwrite.wordpress.com/2014/10/21/book-review
I am a Regulatory Professional, with over 5 years of experience in Regulatory Affairs, and and 10 years of experience writing clinical and regulatory documents. I started this blog as a resource for Clinical and Regulatory Submissions. Medical Device Regulatory Professional. 124; Comments RSS. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Join 41 other followers. Posted on October 21, 2014. Regulatory Intelligence 101 by Meredith Brown-Tuttle. FDA Rec...
TOTAL PAGES IN THIS WEBSITE
12
MedWrite Healthcare Communications
Welcome to MedWrite Healthcare Communications. Healthcare communication across a wide range of therapeutic areas and pharmaceutical brands on different platforms. MedWrite Healthcare Communications is built on a solid foundation of an extensive science background combined with a continuing medical education (CME) and healthcare advertising agency experience. MedWrite Healthcare Communications can help you create communication materials across a wide range of therapeutic areas and pharmaceutical brands.
Medwrite Inc.
Marian Hodges - Medical writer & Editor
I am a freelance medical writer with many years experience working with high quality clients in the pharmaceutical, research and medical communications fields. My writing has covered media ranging from journal papers and conference proceedings, through training packs, product monographs and advisory group meeting reports, to clinical trial reports. I enjoy tackling new subject areas. Some of the subjects on which I've worked are listed below. Sorry, viewing my full CV requires a browser capable of displa...
MedWrite - Publishable Science, Marketable ResultsMedWrite
Customized Scientific and Medical Communications. Supporting Pharmaceutical, Diagnostic, and Device products. For over two decades we have been a trusted vendor to these major pharmaceutical and medical organizations. Our commitment to innovation and excellence culminates long term client relationships. The scientific background and expertise of the MedWrite team. MedWrite-Publishable Science, Marketable Results.
MedWrite Transcription, Inc
Welcome to MedWrite Transcription, Inc. Locally Owned and Operated in Kelowna, BC.
Medical Device Regulatory Professional | A resource for regulatory professionals and medical writers
I am a Regulatory Professional, with over 5 years of experience in Regulatory Affairs, and and 10 years of experience writing clinical and regulatory documents. I started this blog as a resource for Clinical and Regulatory Submissions. Medical Device Regulatory Professional. 124; Comments RSS. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Join 41 other followers. EU pilot on trending. Posted on October 27, 2015. EU pilot on trending. To that end, an a...
Medwritecomm
Research Article Development Services. Books & CME. Study Analyze. Write. Publish. Medwrite’s mission is to collaborate with you. To evaluate, report, and publish your medical evidence expertly and efficiently. Scientific literature is the neural center of medicine. The literature telegraphs research to physicians around the world, influences patient care, and nourishes the medical marketplace. How we can help you. Field of Special Focus. Metabolic / Bariatric Surgery. Our knowledge of the metabolic/bari...
medwritehealthcarecommunications.blogspot.com
MedWrite Healthcare Communications
Wednesday, May 14, 2014. Inside stomach Ramen Noodle digestion goes viral. Tuesday, May 13, 2014. The Panov Program - Precision Chemotherapy / Mt. Sinai Hospital Toronto,. Saturday, September 7, 2013. Mini-review of THE PLAN by Lyn-Genet Recitas. I just bought the book,. THE PLAN by Lyn-Genet Recitas,. After hearing about it on either Dr Oz or some other health-related show. Saturday, June 29, 2013. Monday, June 3, 2013. Canagliflozin: “new class” of diabetes drug approved in the U.S....Canagliflozin - t...
MedWrite Inc | Targeted Messaging for Your Product's Success
Targeted Messaging for Your Product's Success. Regulatory writing for the international pharmaceutical, biologics, and medical device industry for 25 years. MedWrite, Inc. was founded in 1990 by Linda Fossati Wood, RN, MPH, bringing together years of experience in clinical medicine and industry, and an education in study design from Yale University. Creatively express key messages accurately and clearly. Comply with relevant laws and regulations. Site by Round Pond Group.
MedWrite, International: Medical Communications and Event Planning Company
Nurturing Smarter Eating and Healthy Lifestyle Private and Corporate Consultations. Can help you meet your goals. Full-service Medical Communications and Event Management Company. Since 1999 we have been partnering with organizations to develop and execute cutting-edge programs in the following five main service areas:. Medical meetings and event planning. Writing and editorial services. Medical communications, marketing and creative services. Business technology and systems development. Our experts also...
medwritem.com
I write, you cure. Search for posts. Freelance Regulatory & Medical Writing. Has spent over 10 years as a science writer, the last 5 of which were honing the craft of regulatory and medical writing. I bring enthusiasm, talent and perfection to the table. My goals are your goals. My job is to make your job easier. NIH OBA – RAC Appendix M Submissions. Clinical Study Reports (Phases I-IV). ECTD trained and compliant. General Science and Medical:. Peer-reviewed manuscripts and journal publications.
