DICLOFENAC SODIUM BROMINE | IMPORTERS | PAKISTAN
PAKISTAN DICLOFENAC SODIUM BROMINE IMPORTERS AND IMPORT DATA UNDER HS CODE 29224990
Tags:diclofenac sodium buyers in Pakistan,diclofenac sodium importers in Pakistan,pharmaceutical raw material import in pakistan,pharmaceutical raw material importer in pakistan,pharmaceutical raw material buyers in pakistan
DATE | IMPORTER/BUYER NAME | EXPORTER/SUPPLIER | PRODUCT |
30.11.2023 | BOSCH PHARMACEUTICALS (PVT.) LIMITED | AARTI DRUGS LIMITED | Pharmaceutical Raw Material Diclofenac Sodium Brom... |
21.08.2023 | BOSCH PHARMACEUTICALS (PVT.) LIMITED | AARTI DRUGS LIMITED | Pharmaceutical Raw Material Diclofenac Sodium Brom... |
25.06.2023 | M/S FRIENDS PHARMA (PVT) LTD | AARTI DRUGS LIMITED | Pharmaceutical Allopathic Raw Material Diclofenac ... |
8.05.2023 | UNI-TIECH PHARMACEUTICALS (PRIVATE) LIMITED | AARTI DRUGS LIMITED | Pharmaceutical Allopathic Raw Material For Pharmac... |
23.02.2023 | BOSCH PHARMACEUTICALS (PVT.) LIMITED | AARTI DRUGS LIMITED | Desp=-Diclofenac Sodium Bromine Free (Injetable Gr... |
16.02.2023 | ZAFA PHARMACEUTICAL LABORATORIES (PVT.) LIMITED | AARTI DRUGS LIMITED | Diclofenac Sodium Injectable Bromine Free Batch No... |
27.01.2023 | BOSCH PHARMACEUTICALS (PVT.) LIMITED | AARTI DRUGS LIMITED | Pharmaceutical Raw Material Diclofenac Sodium Brom... |
27.01.2023 | BOSCH PHARMACEUTICALS (PVT.) LIMITED | AARTI DRUGS LIMITED | Pharmaceutical Raw Material Diclofenac Sodium Brom... |
26.01.2023 | JAENS PHARMACEUTICAL INDUSTRIES PVT LTD | AARTI DRUGS LIMITED | Description: Pharmaceutical Raw Material Item Name... |
Importing pharmaceutical raw materials into Pakistan involves adhering to specific regulations and procedures set by the government. Here are the general steps and considerations: Registration and Licensing: Importers need to be registered with the Drug Regulatory Authority of Pakistan (DRAP) and obtain a valid license to import pharmaceutical raw materials. Quality Standards: Ensure that the imported raw materials meet the quality standards set by DRAP. They should comply with Good Manufacturing Practices (GMP) and other relevant regulations. Documentation: Prepare all necessary documents, including a commercial invoice, bill of lading, certificate of origin, packing list, and any other specific documents required by customs or regulatory authorities. Customs Clearance: Submit the required documents to customs authorities. Pay any applicable duties, taxes, and tariffs. Customs will inspect the shipment to ensure compliance with regulations. Clearance from Regulatory Authorities: Obtain clearance from DRAP or other relevant regulatory bodies. They might inspect the consignment to ensure it meets quality and safety standards. Transportation and Distribution: Once the consignment clears customs and regulatory checks, it can be transported to its destination within Pakistan. Ensure proper storage and handling to maintain the integrity of the raw materials. Record-Keeping: Maintain accurate records of the imported raw materials as per regulatory requirements. It's crucial to work with experienced import/export agents or consultants familiar with pharmaceutical regulations in Pakistan to navigate the process smoothly. Regulations and requirements might vary, so it's advisable to keep updated with the latest guidelines from DRAP or other relevant authorities.
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