cGMP Manufacturing Services
Audits for cGMP, GMP or other Good Manufacturing Practices don’t have to be stressful if the consultancy you work with focuses on practical systems to do one thing: integrate all reporting in a seamless, effortless automated program.
Smart Pharmaceutical Consulting consultants address GMP, cGMP and other manufacturing practices from our extensive pharmaceutical operations and Quality Assurance experience. From small manufacturing operations to global pharmaceutical giants, we have provided cohesive applications of core regulations to reduce the confusion from interpretive differences by creating seamless GMP programs that assure, when the audit comes, your reporting meets all audition requirements with no “surprises.”
Having automated GMP reporting systems in place is no guarantee your manufacturing practices will be in compliance for an audit. Because SCG consultants stay current with all U.S., European and international cGMP regulations, we can help you can stay ahead of operational compliance changes, making it easier to keep your manufacturing operation in compliance.
Smart Pharmaceutical Consulting’s GMP Training uses real-world case studies to illustrate best practices, helping your company staff work towards more effective implementation of compliance with current Good Manufacturing Practices. This method helps your company build expandable solutions that work today and will continue to help you stay in compliance as your business operation grows.
Ultimately, this level of flexibility in your manufacturing practices will give you a true competitive advantage in today’s increasingly dynamic business environment. Be sure the consultancy you choose is giving you the consulting you need.
If you would like to know more about our cGMP Manufacturing services, please email us at Nigel@SmartPharmaConsulting.com or call us directly at 610-422-1097. We look forward to hearing from you!
If you’ve received a message from the regulatory authority (FDA), we want to help you understand the true intent of the letter. Your company does not want to risk a loss of credibility if this becomes a reality for your organization. Turn to consultants with proven track records in FDA remediation success. Give SPC a call today and let us resolve your specific regulatory issues.