Knowledge Hub

The Indian nutraceutical sector is growing at 15% CAGR. We explore the key ingredients in demand, regulatory landscape under FSSAI, and how manufacturers can build resilient supply chains.

A practical guide to the documentation bundle required for importing pharmaceutical and industrial chemicals — Certificate of Analysis, Material Safety Data Sheets, Drug Master Files, and more.

From MCC starter pellets to enteric-coated PPI systems — an overview of pellet manufacturing technologies, their advantages over conventional tablets, and key quality parameters.

Everything you need to know about Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) — who needs to comply, key timelines, and SVHC restrictions.

How are herbal extracts standardised to guarantee consistent active compound concentrations? We break down marker compounds, HPLC testing, and how to evaluate supplier specifications.

Supply disruptions in 2024 exposed vulnerabilities in dye intermediate sourcing. This piece analyses the causes, their impact on textile and pharma sectors, and practical diversification strategies.

ICH Q3A and Q3B guidelines require manufacturers to identify and control impurities in APIs. We explain the role of certified reference standards in impurity profiling and regulatory submissions.

Food manufacturers sourcing preservatives, sweeteners, and emulsifiers must comply with both Indian FSSAI regulations and EU food additive directives. Here is a side-by-side comparison.