The pharmaceutical industry in Bangladesh has experienced remarkable growth, making significant contributions to the national economy and global healthcare. At the core of this industry lies a complex regulatory landscape that ensures the safety and efficacy of pharmaceutical products. Drug licensing is a pivotal aspect of this regulatory framework, and companies often turn to expert […]
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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)
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In Bangladesh, with its fast-emerging economy and growing industrial base, there has been a corresponding growth in requirements for unique regulatory services. List of Regulatory Service Provider in Bangladesh, Businesses are grappling with an ever growing complex array of legal and regulatory requirements across pharmaceuticals and medical devices, food, cosmetics and chemicals. Government hardens the regulational arteries
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Medical Device Registration Procedure in Bangladesh, The process of medical device registration in Bangladesh is an important regulatory procedure that makes certain all medical devices being marketed and sold in the country are thoroughly reviewed for their safety, quality and performance. Regulated by Directorate General of Drug Administration (DGDA), the registration system upholds public health and is
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How to Becoming 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
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Regulatory in pharma refers to the legal and procedural framework that governs the development, approval, manufacturing, marketing, and post-market surveillance of pharmaceutical products. These regulatory requirements are essential for ensuring the safety, efficacy, and quality of drugs across national and international markets. In the United States, the Food and Drug Administration (FDA) plays a central
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What Is 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. At Zivadra, Regulatory Affairs is at the core of our
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Ziva DRA is a comprehensive regulatory affairs & compliance service provider for the Pharma, IVDs, Medical device & cosmetics industry in the Bangladesh market.
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