Adhering to global and local regulations

Certification & Compliances

We offer a range of products with diversified applications including water treatment, anti perspirants, personal care and more. Each of these is manufactured at sites adhering to cGMP practices stipulated by agencies such as ICH Q7, 21 CFR 210 & 211 and other applicable regulations.

We have obtained the following certifications:

Ensuring compliance at every step

As a leading multinational company, GTI values the guidelines put forward by various regulatory agencies of the countries we do business in. Our expert team is capable of handling water treatment, antiperspirant actives, cosmetics and pharma actives products and also ensuring that we manage various regulatory submissions and compliances stringently. Our team also focuses on adhering to quality standards at site to conform with the requisite guidelines.

Chemical Regulatory Compliance

In recent years, the industry has witnessed significant changes in the legislation pertaining to the manufacture, distribution and supply of chemicals globally. It is crucial to understand the nature of this evolving set of regulations. A comprehensive understanding of all legislation relating to the manufacture, distribution, use, treatment and disposal of chemicals is vital to comply with the regulations. At GTI, our global network of experts experienced in the regulatory domain ensures chemical compliance across all phases of our products’ life cycle.

REACH Compliance

Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) is adopted to improve the protection of human health and the environment from the risks posed by chemicals. It also aims to enhance the competitiveness of the global chemicals industry. A new global norm is to ensure that all the chemicals managed are as per REACH regulations stipulated by regional authorities.

As per REACH, GTI adheres to the following region’s compliance.


Pharma Actives Compliance

Our Pharma Actives team is experienced and well trained in regulatory and quality global standards stipulated by various agencies like FDA, EMEA, CDSCO, WHO etc. It is also proficient in managing various cGMP regulatory standards mandated by regulatory agencies like US FDA 21 CFR 210 and 21 CFR 211, EU GMP Annex II, Schedule M, ICH Q7A, WHO GMP etc.

We extend our knowledge about global and local regulations to our clients. Our team offers end-to-end support on regulatory submissions to our clients and collaborates with them to move forward together.

DMF Filings Details: Under preparation

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