Organizations that manufacture products within a GxP or Regulated environment are required to deliver quality consistently. These companies adopt a Pharmaceutical Quality Management System that ensures Assurance and Control on Quality consistently. But with stringent regulations, growing customer demands and to make a global presence, there is a natural need for the Quality Management System to be robust, effective and efficient..
Implement a comprehensive Batch Manufacturing Record (BMR) system in adherence to quality and Good Manufacturing Practice (GMP) standards. Utilize electronic documentation to trace the entire manufacturing cycle of a batch or lot, ensuring accuracy, compliance, and seamless auditability for quality control and regulatory purposes.
Implement an integrated Inventory and Warehouse Management System for efficient supply chain operations. Utilize software to automate inventory tracking, order fulfillment, and warehouse processes. This solution optimizes stock levels, reduces errors, and enhances overall logistics efficiency by providing real-time visibility into inventory movements and facilitating streamlined warehouse operations.
Establish a centralized Suppliers Directory for efficient vendor management. Utilize a digital platform to catalog supplier information, certifications, and performance metrics. Streamline communication, track deliveries, and manage relationships through a comprehensive and accessible directory. This solution enhances transparency, reduces risks, and facilitates effective collaboration with suppliers.
Implement an Equipment Calibration solution for systematic and accurate calibration processes. Utilize specialized software to schedule, track, and document equipment calibrations. This ensures compliance with quality standards, reduces the risk of measurement errors, and maintains equipment reliability. The solution enhances efficiency by automating calibration workflows and maintaining a comprehensive calibration history for each piece of equipment.
Implement an efficient Batch Processing Record (BPR) Logistics solution in the pharmaceutical industry. Utilize a digital platform to streamline the logistics of BPR creation, approval, and distribution. This solution ensures timely and accurate processing, adherence to Good Manufacturing Practice (GMP), and facilitates a seamless flow of information between manufacturing units, quality control, and regulatory compliance teams.
You can access Pharmaceuticals Standard Operating Procedures (SOP), Guidelines, Analytical Methods, Test Procedures, Instrument Calibrations, and Validation information here.
Listen to what our satisfied customers have to say about their experience working with us and successfully reaching their goals.
Kudos to PharmaMax for their robust quality control (QC) measures. The attention to detail in the testing and inspection processes reflects their dedication to delivering safe and effective products. Trustworthy brand. Dr. Peter Drespel, Forest Laboratories star star star star star_border
Kudos to PharmaMax for their robust quality control (QC) measures. The attention to detail in the testing and inspection processes reflects their dedication to delivering safe and effective products. Trustworthy brand.
Dr. Peter Drespel, Forest Laboratories
Consistency is key, and PharmaMax delivers on that front with their strong QMS and QC protocols. It's reassuring to know that each product undergoes thorough testing, ensuring reliability and compliance. Venkat Kadiyala, Merck Pharmaceutical star star star star star_border
Consistency is key, and PharmaMax delivers on that front with their strong QMS and QC protocols. It's reassuring to know that each product undergoes thorough testing, ensuring reliability and compliance.
Venkat Kadiyala, Merck Pharmaceutical