Sclin Soft Technologies

Sclin Soft Technologies is a USA based company, was

established in 2015, which provides a full range of Clinical
Operations, Clinical Data Management, Bio-statistics,
Medical Writing and Programming Services on customer
friendly business model. Sclin Soft Technologies closely
works with the clients to access their needs and customize a
business model tailor for satisfying their needs. Our
experienced clinically and bio-statistics data management
teams are committed to maintaining. The projects of our
clients on time and within the budget by monitoring the
quality and study of the data real-time performance and
providing meaningful feedback to the project team. Sclin Soft
Technologies data management team will provide a
Customized, Cost effective and Flexible approach to meet the
data management needs.

Medical Writing:
Medical writing is an integral part of clinical research. Our medical
writers work closely with the multidisciplinary teams of the sponsor
i.e, bio-statistic, pharmacological, project management and clinical
data management teams to provide accurate, timely and inexpensive
documents with ethical and scientific standards. Sclin Soft
Technologies offers a complete range of medical writing services for
regulatory submissions, scientific publications and medical-
marketing materials in different therapeutic areas for all phases of the
product from preclinical development to post-marketing literature.
 Sclin Soft Technologies
We guarantee the timely delivery of precise and regulatory-compliant
documents to our sponsors in an affordable and flexible way. We
organize our operations in integrated customer-centric units, to
improve customer focus and to guide operational agility that can lead
to delivery with quality, speed and value.

The medical writers of the Sclin Soft Technologies team receive

regular training to ensure uniformity with regulatory standards and to
have consistency in writing processes. Our medical authors are
scientists involved in the development of drugs that have the required
scientific background, regulatory knowledge and professional attitude
to be incorporated into the sponsor’s study teams during the clinical
development process of a molecule.

Medical Writing Services

1. ICH GCP compliant Clinical study reports(CSR)
2. IND, NDA, ANDA, MAA, CTA Regulatory submission
3. Clinical and non clinical segments of CTD
4. Investigators Brochure
5. Study Protocol
6. SOPs for all aspects of Drug Development process
7. Literature Review
8. Journal articles – Original research, Review articles, Editorials,
case reports, etc.
9. Abstracts – Publication in journals and Submission to medical
meeting

10.Posters Presentation at medical meetings

FOR MORE INFO: https://www.sclintech.com/medical-

writing/