Torbay Pharma Featured in TheBusinessDesk.com!
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Supporting you through your development journey
At Torbay Pharma, we understand the importance of collaboration and open communication when working with our clients. Our approach is built on the foundation of forming genuine partnerships with clients to ensure seamless project execution and satisfaction.
Collaborative and transparent project management
Experienced project managers from our NPI team meet regularly with you from the very beginning of our collaboration. Our experts are responsive, keeping you informed of project developments and empowering you to review and update your projects as needed.
Gap analysis and risk mitigation
We conduct a thorough gap analysis ahead of any technology transfers to identify potential risks. We then conduct feasibility or small-scale studies to understand the product’s behavior and mitigate any risks.
Tailoring to specific client needs
We understand that your project has unique needs and challenges. That’s why we take the time to listen to you to understand your requirements. We are flexible, where it matters, to ensure we can accommodate your needs.
Intellectual property confidentiality
To safeguard intellectual property rights and maintain confidentiality during the manufacturing process, we put non-disclosure agreements (NDAs) and confidentiality disclosure agreements (CDAs) in place with all our clients. We operate in strict accordance with these agreements to protect sensitive information.
Timely delivery strategies
We create detailed project plans for every project, and establish clear scope alignment through project briefs to ensure we deliver for you on time and in full. Regular progress meetings allow us to discuss milestone deliveries with you, and to identify potential risks so we can address them before they become a problem.
By fostering a collaborative, open, and partnering approach, Torbay Pharma strives to exceed client expectations, and establish long-term partnerships built on trust and mutual success.
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 regulations and the current requirements of Annex 1 of the Good Manufacturing Practice (GMP).
Regulatory affairs and QP support
Our dedicated Regulatory Affairs team and Qualified Persons (QPs) assist you in ensuring that 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.
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Sterile supply, made simple
Contact us to learn how we can partner with you to deliver
the sterile supply you need.