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Synowledge Webinar Series:
Register for Webinar on the Importance
of the PV System Master File (PSMF)

 

Synowledge to attend DIA 51st Annual Meeting, Washington DC
June 14th -18th

 

 

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Synowledge specializes in providing Drug Safety, Regulatory Affairs and Clinical services to small, mid, and large sized pharmaceutical, biotechnology and medical device companies. Our experts come with years of experience developing innovative and highly-customizable solutions for life sciences companies of all types and sizes.

Synowledge offers a broad range of Drug Safety and Regulatory Affairs services to help guide pharmaceutical and biotechnology companies through the complex national and global regulatory landscapes. Our highly innovative and customizable solutions are tailored to our client’s specific needs, ensuring the highest level of customization, quality, and compliance. Synowledge also offers Clinical and Biometrics services to help meet the needs of clients in the rapidly growing and increasingly complex life sciences industry.

Our comprehensive outsourcing solutions combine the unique strengths of both onshore and offshore services to help meet all of our clients’ needs, and support the sustained growth of their products.


 
 
     
 
     
 
     
           
 
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Call us:
+1 (203) 504 2561
Email us:
info@synowledge.com
 
 
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