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

As many of the Health Authorities transitioned from paper documentation format to the eCTD format, it is time for organizations to define key…

On-time Regulatory submission is the key to achieve quick time-to-market.

As we all know, each country has its own set of cosmetic regulations that manufacturers must adhere to.

Under the Classification, Labeling and Packaging of substances and mixtures (CLP) regulation, Chemical companies, who wish to place hazardous…

Structured Product Labeling (SPL) and Structure Product Monograph (SPM) are the mandatory document mark-up standards for the submission of label…

Drug development is an extensive and multifaceted process.

The life sciences industry is ever-changing and evolving. It’s the same in the year 2018.

As popularly known, IDMP (Identification of Medicinal Products) can be defined as a set of common global standards and technical specifications of…