Modifications in regulations by leading bodies such as the US Food and Drug Administration (USFDA), WHO, CFDA, Health Canada, and the European Medicines Agency (EMA) have magnified the significance of regulatory compliance management for drug manufacturers.

Pharma companies across the globe are required to change their compliance practices to conform to changes in regulations and stringent anti-corruption laws. The US FDA oversees regulatory activity across the globe making pharma & life sciences companies identify quality issues before they impact production.

With the FDA and other regulators broadening the scope of compliance requirements, it helps if companies have a holistic approach and make regulatory compliance part of the corporate strategy along with competent consultants and service providers proficient with quality and compliance.

Xcel Lifesciences help to change your enterprise’s compliance practices to adopt new changes in regulations and stringent anti-corruption laws.

We help with four validation types such as,

• Analytical method validation
• Process validation
• Cleaning validation
• Equipment validation