Resource Pool:

 

Developing and marketing medical products requires a constant output of high quality scientific writing. AccuScript has an experienced team of writers with clinical, medical, and regulatory expertise to help life science companies document efficacy and safety and stay in compliance worldwide throughout the product lifecycle. 

 

The team possesses strong analytical and interpretation skills, comes with a thorough knowledge of experimental design and biostatistics, demonstrates good exposure to standard editorial/ style conventions, and is highly proficient in computer word processing programs. Writers who lead and manage the teams are hand-picked and remain hands-on considering the domain-intensive nature of the job.

 

Training:

 

Our medical writers:

 

 

• Undergo a comprehensive training plan for induction, which includes a medical writing mock-project, guided and evaluated by the advisor of AccuScript Solutions, Dr. R. Chawla

 

• Are compliant with FDA and  EMEA regulatory requirements

 

• Are trained on ICH principles for Clinical trials

 

• Are familiar with Endnotes and medical dictionaries

 

• Sign a confidentiality agreement with our company, under which they cannot disclose any clinical trial data to anyone outside AccuScript

 

• Have their highly reliable service readily available, and can meet tough deadlines with the perfect accuracy of work that they are trained to deliver

 

Data Security:

 

We understand the criticality of confidentiality of information & data security in medical writing for our clients.

Hence our IT security procedures are benchmarked with best practices across the globe:

 

• Physical security and biometric access control for server/archival rooms

• Efficient disaster recovery and business continuity planning

• Security of clinical study data ensured by use of Firewall, and TLS encryption for emails & IPSEC for business to business secure virtual private network (VPN)