Your own dedicated project management team
For more than 25 years, Bellwyck has been a true partner in developing smarter solutions for the pharmaceutical industry — from clinical trial to commercialization. Our consulting services start with a dedicated project management team led by a single point of contact throughout your project.
Cold-chain logistics expertise
Our GMP-compliant storage capacity, cold-chain logistics expertise and global distribution capabilities means we can fulfill your unique needs no matter the size or scope of your project.
While regulatory compliance is a major driver for serialization projects, breaches to the Pharmaceutical Supply Chain distribution system are also a concern, as they can pose health risks to patients and financial risks to the supply chain stakeholders. At Bellwyck, our holistic and comprehensive approach to serialization ensures these risks will be mitigated and will maximize your value.
Our experience with DEA Schedule II-V controlled substances and Class I and II chemicals will ensure your product’s integrity and security remain intact. We will serve as your partner with reliable supply chain solutions that will ensure compliance in this strict regulatory environment.
Our GMP-compliant storage capacity, cold-chain logistics expertise and global distribution capabilities means we can fulfill your unique needs no matter the size or scope of your project.
We understand that labeling and packaging your trial drug is an intricate and vital piece of your project. While the clinical supplies packaging industry has changed substantially over time, we make sure our experts keep up-to-date and understand how these changes affect your packaging needs.
For more than 25 years, Bellwyck has been a true partner in developing smarter solutions for the pharmaceutical industry — from clinical trial to commercialization. Our consulting services start with a dedicated project management team led by a single point of contact throughout your project.
For more than 20 years, Bellwyck has been a true partner in developing smarter solutions for the pharmaceutical industry — from clinical trial to commercialization. We utilize cost-efficient packaging strategies to launch clinical studies on time, every time. Discover all of the ways in which Bellwyck might assist you in meeting your unique objectives.
DEA Schedule II-V
Ensuring that your clinical trial goes smoothly is our priority, particularly when controlled substances are involved. A large part of the complex support required for clinical trials using scheduled drugs is understanding and having the skill to navigate the regulations surrounding them.
While regulatory compliance is a major driver for serialization projects, breaches to the Pharmaceutical Supply Chain distribution system are also a concern, as they can pose health risks to patients and financial risks to the supply chain stakeholders. At Bellwyck, our holistic and comprehensive approach to serialization ensures these risks will be mitigated and will maximize your value. We have partnered with industry leader Optel Vision to provide you with a flexible serialization solution that can meet a wide range of requirements.
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