All pharmaceuticals, surgical products, diagnostic products and health supplements are regulated by the Cosmetics, Devices and Drugs Authority (CDDA) which is the body appointed by the Ministry of Health of Sri Lanka for regulation of both locally manufactured and imported products. It is mandatory to register all products falling under the above categories with the CDDA by fulfilling the stringent regulatory requirements laid down by the CDDA before such goods can be imported into the country / marketed in the country. The duration taken for registration a new product can vary depending on the compliance with the stringent documentation requirements and procedures followed by the CDDA.
With over 60 years experience in the field of pharmaceuticals, Hemas has mastered the regulatory environment to ensure new product registrations in record timing. The Regulatory Division of the company employs highly qualified professionals with a wealth of experience and expertise and very strong understanding of all requirements and procedures. This ensures our Principal organizations are well guided in new product registrations and registration renewals.
Hemas has demonstrated its capabilities in this crucial area of the business while maintaining an untarnished image for its high ethical standards in the industry.