MANUFACTURING FACILITIES
MedCare produces pharmaceutical results of various dose shapes in an assembling plant as affirmed in the Biological and Non-Biological Drug Manufacturing Licenses gave by the Licensing Authority, Drugs (Directorate General, Drug Administration) of Bangladesh and restored at regular intervals after examination by the position.
MedCare has a well-arranged structure with devoted and isolated squares for general items and cephalosporin items. The assembling plant is overseen by a gathering of expertly qualified drug specialists, scientific experts and microbiologists and worked by a well-prepared and qualified work power. The activity is finished guaranteeing severe consistence with cGMP rules, winning national and worldwide models as per the pharmaceutical business. Wellbeing and security of the workforce during activity and ecological assurance is a fundamental piece of the quality procedure.
The assembling plant is situated at BK Bari of Gazipur, around 45 km from Dhaka city and 2.5 km from the western side of Dhaka-Mymensingh expressway. The site region is around 7 sections of land with 5800 sqm of secured zone. The site approaches national force and has its own profound cylinder well for satisfactory water supply. The general utilities incorporate steam, packed air, power back-up and profluent treatment plant.
1. Quality Assurance
Quality affirmation during generation and quality control is the way in to the predictable creation of greatest claim to fame items. The organization has an exhaustively structured and effectively actualized arrangement of value affirmation fusing current Good Manufacturing Practices, Quality Control and Quality Risk Management to accomplish its quality target dependably. Documentation, consistence, deviation announcing and restorative and preventive activities are rehearsed enthusiastically.
2. Production
Maintaining proper documentation and utilizing modern production machinery and equipment different dosage forms like tablets, capsules, liquid filled capsules, powders, creams, ointment, lotion and oral liquids are manufactured in segregated areas to consistently produce products of highest quality. Well defined standard operating procedures (SOP) in compliance with the procedures and instructions of ISO 9001 guidelines are followed and documented in batch manufacturing records incompliance with the cGMP.
3. Product Development
Advancement of marked nonexclusive items is given exceptionally high significance in the association. Item Development Department is outfitted with every single required office and oversaw by a group of qualified work force. They are answerable for structuring definition, creating fabricating procedure and undertaking dependability to create items which satisfies high guidelines and reliable quality.
4. Quality Control
Quality affirmation during generation and quality control is the way in to the predictable creation of greatest claim to fame items. The organization has an exhaustively structured and effectively actualized arrangement of value affirmation fusing current Good Manufacturing Practices, Quality Control and Quality Risk Management to accomplish its quality target dependably. Documentation, consistence, deviation announcing and restorative and preventive activities are rehearsed enthusiastically.
