Regulatory Services

Our Services

Intelly RegoCom offers its services in Ingredient Science, Product Compliance, Product classification across categories, Ingredient or Product approval, Claims substantiation, Nutrition labelling, Import clearance, Licensing and Registration, training, documentation and technical submissions.

Regulatory Strategic Services

Regulatory Strategic Services

The compliances for any product starts from sourcing the correct ingredient to its manufacturing, labelling and finally the launch of product in the market. IRC will help you from end to end process in product development. Once the product is manufactured with due diligence, the clients are supported with labelling services and artwork compliances of the product.

IRC also evaluates and provides guidance on all the aspects of regulatory strategy for product development, product approval, Licensing and Registrations of the manufacturing of the plant.

Product Classification

Product Classification and Ingredient Analysis

Some health supplements present in the global market while entering in India are required to be referred as Nutraceuticals as per Health supplements and Nutraceutical Regulations. The Regulations sometimes add a possible ambiguity in the nomenclature of Health Supplements and Nutraceuticals.

IRC offers review of the products for its appropriate classification under various categories like Health Supplements, Nutraceuticals, FSMP and FSDU etc.

Nutrition Labelling

Nutrition Labelling

Labelling Regulations in India are undergoing frequent changes and becoming increasingly stringent. In such case, it becomes quite challenging for the organizations to ensure that the labels are in compliance with the constantly evolving Regulations.

IRC provides comprehensive nutritional labelling services to ensure that the product labels are fully compliant with Indian Regulations.

Claims Substantiation

Claims Substantiation

We review and offer recommendations on the claims of the products to help you effectively deliver your message to the consumer while also meeting the statutory and regulatory requirements.

It’s our years of experience in the Indian market which has helped us to understand the types of the claims which are usually allowed in the Indian health supplement industry by the federal regulator.

Another important aspect of claims which we offer is the clinical assessment of health claims approval. IRC simplifies the often time consuming process by helping you to prepare, submit and assist in the submission to the authority.

Import Entry Assistance

Import Entry Assistance

Food Safety and Standards Authority of India have notified the Food Safety and Standards (Import) Regulations in 2017 to streamline the process of clearance of imported food in an efficient and transparent manner.

  • We help our clients in applying for food import license in FSSAI and Import Export Code (IEC) from DGFT.
  • Provide assistance in evaluating the import documents like CoA, label compliance etc.
  • Assist in getting Sanitary import permit (SIP)/ Plant quarantine information system (PQIS) as per the product.
Training and Webinars

Training and Webinars

To keep up the pace of the continuously changing regulatory environment, it is important to be aware of the developments in the industry. The best way to be well informed is to keep learning and acquiring the latest skills by appropriate training.

According to the provisions under FSS Act, 2006, the Food Safety and Standards Authority of India must ensure training of the persons who are involved in food businesses.

  • IRC is competent and experienced to provide trainings on GMP practices specific to the Health supplements and Nutraceutical sector.
  • IRC also provides trainings on Nutraceutical Regulations, artwork and labelling compliances and product compliances.
Documentation Process

Documentation Process and Technical Submissions

The process of documentation preparation should be in such a way that it reduces the possibility of queries by the authorities. IRC provides strong support in developing and managing technical documents which make the approval process easier for the products.