As the premier Contract Manufacturer of wet wipes on a global level, we are the wet wipe experts. We are a full service turnkey organization that can take care of everything from sourcing raw materials, to developing the ideal formulation to manufacturing a high quality finished product that is ready to go.
Once the project is ready to advance from concept to execution, the Product Development team takes the lead. Working closely with our customer and with PDI's R&D, Regulatory, Operations and Quality support groups, the team is charged with all aspects of bringing the product to market. Once the product has been commercialized, our Customer Support team takes over and manages the ongoing business.
From product concept to product launch to product support, our project leadership teams are vested in your business and clearly understand that our success is based on our customer’s success in the market.
Quality comes first as stated in our Guiding Principles. We operate our facilities in accordance with the Code of Federal Regulations and have the following certifications and registrations:
- ISO 9001:2008
- ISO 13485:2003
- FDA Registered
- EPA Registered
At PDI, our Quality System is founded and built with a focus on cGMP and industry best practices. Our system dictates compliance from incoming raw materials through finished goods testing. We utilize quality personnel throughout our facility and are brought in on new projects at the very beginning. Our Quality Department has numerous in-house capabilities and resources such as micro and analytical labs, document control experts, engineering and validation teams, and most importantly, the support of the ownership of the organization.
We invite you to contact us to learn more about our approach and how we can work together on your product. We understand that quality cannot be inspected into a product; rather it takes a commitment from everyone in our organization.
PDI Contract Manufacturing offers a complete and vast array of services to support our customers. This includes full validation services starting with bulk liquid processing, continuing through the packaging process, and ending with cleaning and sanitization. These validations are performed in alignment with latest FDA Process Validation Guidelines along with cGMP. We also offer the following services:
- Formula Development
- Preservative Testing
- Package Stability
- Clinical/Safety Testing
- Accelerated and Real Time Stability Testing