আমাদের দেশে বেশ কয়েকটি চিকিৎসা পদ্ধতি প্রচলিত রয়েছে। সবচেয়ে বেশি ব্যবহৃত চিকিৎসা পদ্ধতি হলো এলোপ্যাথি। একে আধুনিক চিকিৎসা পদ্ধতিও (Modern system of medicine) বলা হয় ৷ অন্য যে পদ্ধতি গুলো এখানে আছে এবং অনেক মানুষ এসব পদ্ধতির চিকিৎসা গ্রহণ করে থাকে সেগুলো হলো: (ক) আয়ুর্বেদিক (Ayurvedic)(খ) মঘা (Mogha)(গ) ইউনানী (Unani)(ঘ) হোমিওপ্যাথি (Homeopathy)(ঙ) বায়োকেমিক (Biochemic)(চ) আকুপাংচার…
To start the business development of APIs in Bangladesh, you should have the source validation registration in DGDA Database. DGDA stands for Directorate General of Drug Administration, responsible for control and regulate the pharma and medical device industry of Bangladesh. If Pharma DRA holds the API source validation certificate for a foreign API manufacturer outside…
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A successful registration and smooth registration process depends on the right classification of your medical device with any regulatory authority. We developed this database for the convenience of the global medical device manufacturers for Bangladesh market access. Local distributors and importers can get an idea by searching their products in our database. *This database is…
For import into Bangladesh: Following are the Govt. fees for various types of medical device registration: Class A: No Govt. fees required. Class B, Class C and Class D: BDT 63,250 per product Following are the Govt. fees for various types of IVD reagents and instrument registration: Class A: No Govt. fees required. Class B,…
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A local representative/Local agent/Local indenting firm is mandatory for holding the registration (i.e., API Source validation) in Bangladesh. We are the source validation registration holder of APIs of 1. Glochem Industries Pvt. Ltd., Hyderabad, India 2. Chemeca Drugs Pvt. Ltd., AP, India 3. Hetero Drugs Ltd., Hyderabad, India 4. Liford Pharma LLP, Gujarat, India Contact…
According to the Drug and cosmetics act, 2023, IVD reagents, instruments and analyzers are under the jurisdiction of Directorate General of Drug Administration, Bangladesh. IVD reagents are classified as Class A, B, C and D in the medical device guideline of Bangladesh. DGDA is the regulatory authority for the IVD reagents and rapid test kits….
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