Torbay Pharma Featured in TheBusinessDesk.com!
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Tech transfer and scale-up made simple with technical assessment support
Torbay Pharma offers comprehensive technical assessment to support your contract manufacturing projects. With our in-depth product development and analytical testing support, we can help you identify and solve potential project risks and challenges.
We are committed to forming genuine partnerships with you, harnessing our niche product experience to understand your needs in order to devise a tailored solution for your project.
Key services
Our technical assessment can support:
- Horizontal technology transfer – Transferring your product to Torbay Pharma from another manufacturing site where it is already commercially marketed
- Scale-up from development to commercial – Taking your newly-developed product and establishing formulation, process and analytical methods to scale up for commercial production
- Full drug development – Identifying formulation, process and analytical methods to generate a data package for licensing through to commercial sale
Your project is in reliable hands
Our team of technical experts has extensive experience in contract manufacturing for sterile injectables and oral liquids. We have worked with a range of clients with a proven track record of success.
Scale up and speed up
With our technical assessment experience, you can benefit from:
- Reduced risk: Identify potential risks and challenges early on in the project, so that you can take steps to mitigate them.
- Increased efficiency: With our detailed assessment at the beginning of your project, we can help you streamline your journey and avoid costly delays.
- Peace of mind: Our assessment can give you assurance, knowing that your project is in reliable hands.
Quality and compliance
Our skilled team are experts in global regulatory standards, helping to ensure your sterile supply simply meets the highest quality and compliance requirements.
Compliance with quality standards
We ensure compliance with the current requirements of EU Good Manufacturing Practice (GMP).
Regulatory affairs and QP support
Our dedicated Regulatory Affairs team and Qualified Persons (QPs) assist you in ensuring your supply of licenced medicines, specials or investigational medicinal products (IMPs) have the required documentation for regulatory compliance.
Our facilities
Our state-of-the-art 78,500-square-foot facility offers cutting-edge infrastructure to meet your unique needs. We invest in the latest equipment to respond as your requirements change.
Production agility
We can adapt our production output, minimizing lead times, ensuring uninterrupted supply.
Volume flexibility
We can support a range of projects, from small- to medium-sized batches.
Customer support
Our customer support team can guide you in accessing and exporting our products.
Expertise in exporting to other markets
We are experienced in shipping to other markets, and can support you in exporting in compliance with all applicable laws.
Assistance with documentation
We can provide the necessary documentation with each shipment, including certificates of origin and export licences.
Single point of contact
We offer a dedicated team member to support you in meeting all of your manufacturing and shipping needs.
Sterile supply, made simple
Contact us to learn how we can partner with you to deliver
the sterile supply you need.