How to Setup Pharmaceutical Company in Bangladesh The pharmaceutical sector of Bangladesh is expanding at a fast pace, making a significant contribution to the national economy and health system. Bangladesh has more than $3 billion worth of potential market for domestically produced pharmaceutical products and a huge market in export is also waiting in USA, Europe and […]
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Regulatory affairs ensure businesses comply with laws, protect consumers, and foster trust. It is vital for industries like pharmaceuticals, food, and cosmetics. In Bangladesh, Ziva DRA stands out as a trusted regulatory consultancy, guiding businesses through complex requirements with expertise and precision. That is why, in this article, we will explore regulatory consultancy services, and
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In the ever-evolving business landscape of Bangladesh, where innovation meets tradition, the role of business consultants has become increasingly pivotal. This article aims to delve into the multifaceted world of Business Consultants in Bangladesh, shedding light on the comprehensive services offered by consultants, with a spotlight on Ziva DRA‘s expansion into this dynamic field. Understanding
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In the vibrant tapestry of Bangladesh’s business landscape, where commerce thrives and industries flourish, obtaining a trade license is a crucial step for businesses seeking legitimacy and compliance. This article explores the pivotal role of trade license consultants in Bangladesh, with a particular focus on Ziva DRA’s expansion into trade license consultancy. Understanding Trade Licensing
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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. 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 and get domestic standards closer (in sync)to
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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 &
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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 crucial
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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
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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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