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Top 5 Challenges in Pharmaceutical Regulatory Submissions and How to Overcome Them
Regulatory submissions are a critical step in bringing pharmaceutical products…
The Role of Quality Management Systems (QMS) in Pharma
In the pharmaceutical industry, ensuring the safety, efficacy, and quality…
Understanding the New EU Medical Device Regulations (MDR)
The European Union’s Medical Device Regulation (EU MDR) represents a significant shift…
How to Prepare for a Successful FDA Audit
An FDA audit is a critical event for any pharmaceutical…
The Importance of Good Manufacturing Practices (GMP) in Pharma
In the pharmaceutical industry, ensuring the safety, efficacy, and quality…
Navigating Global Regulatory Compliance: A Guide for Pharmaceutical Companies
The pharmaceutical industry is one of the most heavily regulated…
Good Manufacturing Practices (GMP) for Natural Health Products in Canada
Introduction Natural Health Products (NHPs) are a cornerstone of health…
Understanding Self-Care Products in Canada: What You Need to Know
Introduction Self-care products are an essential part of our daily…
How to Register and Create business profile on NSWS ( National Single Window System)
NSWS is established by the Central Government with the objective…
Whether all Medical Devices are regulated under the Medical Devices Rules, 2017?
Yes, as per the notification S.O. 648 (E) dated 11.02.2020,…