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Streamlining Regulatory Submissions Through Data

Pharmaceutical professionals in the Regulatory space face complicated, rigorous, and ever-evolving requirements for the Regulatory approval of…

November 11, 2022
eDMS - The driving force for Successful Regulatory Operations

Life sciences is a highly regulated industry, full of sensitive information that is required to be maintained efficiently.

November 7, 2022
Automating Medical and Scientific Literature Monitoring  for Drug Safety (PV)

Pharmacovigilance safety database systems are crucial in today’s Life Sciences world, where ensuring data quality is integral to help simplify the…

October 28, 2022
eCTD 3.2.2 Vs. eCTD 4.0 - How Significant is the Change?

eCTD has turned into a standard norm for industry-wide submissions in a majority of regions across the globe.

October 13, 2022
Automated Regulatory Intelligence (ARI): Keeping you Ahead of the Curve

Regulations stand crucial for any industry that functions in the Life Sciences domain, which is the third most heavily regulated sector after the…

September 15, 2022
EMA IDMP-SPOR Implementation Guideline v2.1.1 – A Brief Review

On July 28, 2022, the EMA released an incremental update to the IDMP-SPOR implementation guide (IG).

August 29, 2022
Regulatory Intelligence (RI): The Focal Point of Your Business

Introducing innovative products across global marketplaces is imperative for life sciences companies to ensure profitability and maintain their…

June 29, 2022
Revolutionize Regulatory Publishing & Submission with Automation

For years, Regulatory publishing was done by manual tasks.

April 27, 2022
Stay on Top of New Global Regulatory Guidelines with Data-driven Regulatory Intelligence

Life science companies face massive challenges while constantly staying ahead of dynamic Health Authority (HA) updates.

April 19, 2022
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