Document management for global standards and regulations
Audit, accounting and advisory
Document management for global standards and regulations Get white paper
Document management for global standards and regulations Get white paper
Audit, accounting and advisory View industry
Going beyond GMP – assuring quality in the generic drug industry
Explore how pharmaceutical companies can optimize their GMP processes with a QMS solution to address the challenges of the "patent cliff," improve consumer trust, and increase revenue.
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Enhancing GMP compliance in the generic drug industry
The loss of revenue due to patent expiration, known as the "patent cliff," forces pharmaceutical companies to make key changes. This white paper outlines how companies can enhance GMP processes to mitigate risks and build market reputation.
Why you need this whitepaper
Learn strategies to enhance quality standards and ensure compliance in the generic drug industry.
Prioritize high standards
Dive into the importance of maintaining high-quality standards and the benefits it brings.
Understand compliance risks
Learn about the consequences of non-compliance with GMP and poor quality practices.
Leverage QMS solutions
Discover how QMS software can unlock compliance, quality, and improvements across your pharmaceutical business.
Mitigate patent cliff risks
Gain insights into strategies to address potential issues surrounding the patent cliff.
Don’t miss out on these valuable insights
Whether you’re curious about features, pricing or implementation we can help you found the right solution for your business.
Whether you’re curious about features, pricing or implementation we can help you found the right solution for your business.
Whether you’re curious about features, pricing or implementation we can help you found the right solution for your business.
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