For years, Regulatory publishing was done by manual tasks.
Life science companies face massive challenges while constantly staying ahead of dynamic Health Authority (HA) updates.
In addition to completing the requisite xEVMPD data submissions, life sciences organizations will now need to use a web-based application form…
The world of life sciences is ever-changing and becoming more challenging, with fast-paced Regulatory guidelines being introduced frequently.
The post-pandemic world is realizing that the intersection of technology and a traditional way of doing business already exists with us.
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.