The Regulatory Environment in Sri Lanka
The National Medicines Regulatory Authority (NMRA) regulates all pharmaceuticals, surgical products, diagnostic products and health supplements. This organization is 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 NMRA by fulfilling the stringent regulatory requirements laid down by the NMRA before such goods can be imported into or marketed in the country. The duration taken for registration of a new product can vary depending on the compliance with the stringent documentation requirements and procedures followed by the NMRA.
Our six decades of experience as the pre-eminent distributor of the healthcare industry has given us all the needed experience for fast-tracking new product registrations. We have employed an incredibly adroit team in our Regulatory Division, the members of which have mastered the regulatory environment to secure new product registrations in record timing. This deep understanding safeguards our principles throughout the registration process, ensuring professional guidance every step of the way. We adhere to the highest ethical standards in all of this division’s operations, enabling us to preserve our untarnished reputation as an honest corporation.