PRODUCT REGISTRATION

Regulatory Affairs ensures compliance with the requirements of national and international authorities. This helps us to ensure that our products meet the required standards. Our regulatory affairs team develops regulatory strategy and integrates legal constraints into product development plans. Moreover department ensures that the firm adheres to the laws protecting public health.

Licensing for internation products
Increasingly, many other countries also require the registration of pharmaceutical and medical devices with their local regulatory bodies before importation. Imperia Pharmaceuticals Pvt Ltd is committed to fulfilling all regulatory requirements by registering our products as required in the markets where we operate. We aim to be one of the first companies to do so.

International Registration
ILS recognised the value of registrations long before developing nations first imposed them and, as a result, our registration dossiers is submitted and processed well ahead of many other pharmaceutical suppliers.
Achieving registrations can be a complicated process and each country has its own requirements. Our adherence to UK and EU standards mean that we are well-equipped to meet requirements for international markets. Our regulatory team has the knowledge and expertise to compile registration dossiers for pharmaceuticals and medical devices for many countries around the world.
We work closely with National Competent Authorities in order to collate the appropriate documentation and samples and we combine first-hand knowledge with our own regulatory team to achieve the speedy process of each dossier.
When full product registration is not required, we can supply internationally recognised, WHO format Certificates of Pharmaceutical Product (COPP) and other similar documents which may be required for importation.
ILS supports these regulations and assists various governments with the process, on behalf of our customers, in order to meet the health demands of their population. ILS has registered hundreds of our pharmaceuticals and healthcare products worldwide. Being a highly detail oriented process, product registration procedures and requirements vary according to country.
ILS works with various government, ministries, agencies, and administration to ensure that our products can serve the health needs of their people and animals.
We strive to work with likeminded partners who are attuned to local regulatory requirements, to assist the speedy completion of registrations.