M Polash Islam

In the intricate landscape of regulatory compliance within Bangladesh’s pharmaceuticals, medical devices, cosmetics, and food industries, businesses face multifaceted challenges. This blog post delves into the pivotal role of regulatory consultants in alleviating these challenges, with a focus on Ziva DRA, a leading regulatory service provider in the country. Understanding the Regulatory Landscape in Bangladesh […]

Directorate General of Drug Administration (DGDA) is the drug regulatory authority in Bangladesh. In the realm of healthcare, ensuring the safety and efficacy of drugs is paramount. This responsibility falls upon the shoulders of drug regulatory authorities, who play a critical role in safeguarding public health. In Bangladesh, the Directorate General of Drug Administration (DGDA)

There is the list of Comprehensive regulatory service provider companies in Bangladesh- Ziva DRA Bangladesh’s burgeoning economy, characterized by rapid growth and expansion, has inevitably led to an increased demand for regulatory services. These services are crucial for ensuring that businesses adhere to the nation’s legal framework and maintain compliance with industry standards. While the

Medical device registration in Bangladesh involves a strict and detailed procedure that must be followed. This process ensures that medical devices meet the necessary safety and quality standards before they can be sold and distributed in the country. List of required documents for medical device registration in Bangladesh: Legal agreement (copy) between the manufacturer &

To become a regulatory affairs specialist, you need a minimum of a bachelor’s degree in a related field and experience working in regulatory compliance or a similar role. Additionally, obtaining certifications such as RAC (Regulatory Affairs Certification) can enhance your career prospects and demonstrate your expertise in this field.   Regulatory affairs specialists play a

Regulatory in pharma refers to the set of laws and guidelines that govern the development, production, and distribution of pharmaceutical products. The pharmaceutical industry is highly regulated to ensure the safety, efficacy, and quality of drugs.   Regulatory bodies, such as the Food and Drug Administration (FDA) in the United States, play a crucial role

Regulatory Affairs in medical devices involves ensuring compliance with regulations and standards set by governing bodies for the safety and efficacy of medical devices. Medical device companies navigate through a complex landscape of regulations to gain approvals and maintain compliance for their devices.   This process includes preparing and submitting regulatory submissions, managing product labeling,