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.
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.
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. Which is why we assist in identifying the correct nomenclature for the product. Because it’s vital to use the correct nomenclature on the label to avoid enforcement issues and provide mandatory compliances as per the product classification.
IRC offers review of the products for its appropriate classification under various categories like Health Supplements, Nutraceuticals, FSMP and FSDU etc.
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. Labels are an important part of the product packaging. It is used to provide correct information regarding the product.
IRC provides comprehensive nutritional labelling services to ensure that the product labels are fully compliant with Indian Regulations.
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. Referring to those legal provisions, we evaluate and offer guidance for claims regarding the substantiation of the claims on labels.
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. Reputed clinical trial agencies are associated with us in providing end to end support for the claims.
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. It is imperative for the health supplement market to be regulated. The importers must exercise due diligence and ensure to self-regulate when importing health supplements and nutraceuticals into the country. It is vital that an importer must ensure to import only such products which comply with FSSAI defined Standards and Regulations.The imported supplements undergo the process of screening in which we can assist for the smooth launch of your product in the market.
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 (manufacturing, packaging, storage and transportation), whether as food business or as employee or otherwise.
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. We aim to make the process of product-launching as hassle-free and efficient as possible.