Purpose-built ERP software for Pharmaceutical Manufacturers
Compliant Manufacturing for Critical Products
Whether you're manufacturing APIs, finished dosage forms, or pharmaceutical intermediates - you need ERP software for the pharmaceutical industry that supports GMP compliance and regulatory requirements. Klipboard Manufacturing provides the batch control, traceability, and documentation your industry demands.
- Our role in your industry
- The challenges you face
- Benefits of Klipboard Manufacturing
Our role in your industry
Klipboard's Role in Pharmaceutical Manufacturing
At Klipboard, we understand that pharmaceutical manufacturing operates under the most stringent regulatory frameworks. Our ERP systems for pharmaceutical manufacturing supports GMP requirements, batch record documentation, and the quality systems regulatory compliance demands.
By integrating formulation management, production control, and quality systems, Klipboard delivers ERP for the pharmaceutical industry that helps manufacturers maintain compliance, ensure consistent product quality, and manage documentation efficiently.
The challenges you face
We Understand the Challenges You're Facing
You're not just making pharmaceuticals - you're operating under regulatory frameworks that demand validated systems, complete batch records, and comprehensive quality documentation. We work with pharmaceutical manufacturers every day, so we understand the reality you're facing:
- GMP Compliance and Regulatory Requirements: FDA, MHRA, and other regulatory requirements demand comprehensive systems. Maintaining compliance while running efficient operations is a core strength of the best ERP for the pharmaceutical industry.
- Batch Record Documentation: Complete batch records must document every aspect of production. Capturing all required data while maintaining production flow is challenging without integrated systems.
- Formula and Process Control: Formulas, recipes, and process parameters must be tightly controlled. Managing formulation changes, deviations, and validation status requires structured workflows supported by ERP systems for pharmaceutical manufacturing.
- Quality System Integration: Quality systems must integrate with production operations. Managing specifications, recording test results, and handling deviations and CAPA requires connected processes.
We've seen it, we've heard it - and we've built Klipboard Manufacturing to help you take control of it.
Benefits of Klipboard Manufacturing
Klipboard Manufacturing: Built for Pharmaceuticals
We don't just tick boxes. We solve the everyday challenges pharmaceutical manufacturers face with ERP for pharmaceutical industry operations that support GMP, quality, and regulatory compliance.
Batch Control and Traceability :
Track materials and components with full lot traceability. Maintain the batch genealogy required for regulatory compliance and recall capability.
Formulation Management:
Manage product formulas with controlled revision processes. Track all changes with full audit trails to support validation requirements using ERP systems for pharmaceutical manufacturing.
Production Documentation:
Capture production data to support batch record requirements. Record process parameters, quantities, and operator actions with timestamps.
Quality Data Integration:
Record test results and specifications against batches. Support deviation management and CAPA processes through integrated quality workflows using the best software for pharmaceutical industry ERP environments.
Material Management:
Manage raw materials with status control and expiry tracking. Maintain supplier qualification records and material certifications.
The Numbers Behind Klipboard
50,000
Global Customers
320,000
Daily users
74
Countries
100,000
Orders processed daily
More From Klipboard
Speak to an Expert Today
Talk to one of our manufacturing specialists to find out how our ERP solutions can help your business.
Get in Contact with Us
Fill in our contact form to have one of our team of experts contact you about our range of solutions.
