Blogs

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

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

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

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

On July 28, 2022, the EMA released an incremental update to the IDMP-SPOR implementation guide (IG). The latest version, 2.1.1, addresses a few…

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

For years, Regulatory publishing was done by manual tasks. Publishers used to work for hours formatting documents, generating Agency-compliant…

Life science companies face massive challenges while constantly staying ahead of dynamic Health Authority (HA) updates. In addition, it requires…

In addition to completing the requisite xEVMPD data submissions, life sciences organizations will now need to use a web-based application form…

The post-pandemic world is realizing that the intersection of technology and a traditional way of doing business already exists with us.

The world of life sciences is ever-changing and becoming more challenging, with fast-paced Regulatory guidelines being introduced frequently. Over…

While creating compliant packaging, controlling the labeling flow and its implementation through artwork, supply chain and printing involves…