It is important to know that GMP, GDP and ISO requirements are not regulated procedures but general guidelines that every organization needs to comply with as it sees fit and the nature of activities carried out. There are many ways in which these requirements may be implemented, and it is the organization’s responsibility to determine the most effective way to create this into a high quality process. Ultimately, a proper quality system must ensure the quality of the medical product in order to safeguard its consumer’s health.

It should be emphasized that the Health authorities conduct regular audits for suppliers of health services such as manufacturers, importers, drug warehouses and laboratories, and if significant impairments are found, sanctions or even legal procedures for stopping business activity may be imposed until the impairments are corrected.

Barrco Regulatory Solutions provides services based on vast theoretical and practical knowledge in the quality and QC fields, high professionalism, high flexibility to changes, uncompromising quality of performance, and assists our clients to benefit from our experience and withstand high standards set by the health authorities.

Together with the professionalism of the company employees and their proven methods of work Barrco Regulatory Solutions will enable you to be sure that this critical activity is performed according to the Health Authorities requirements and your expectations.

We are aware that the responsible pharmacist is the central link in the process of supplying healthcare products at the required quality in order to maintain the safety in the patients, and its success is dependent on maintaining an excellent working relationship with the manufacturers, drug warehouses, transporters and of course, the inspection unit of the Health Authorities.