A Comprehensive Ecosystem of Regulatory Partners & Solution Providers
Whether your team needs specialized nonclinical, clinical, or CMC support, regulatory publishing expertise, manufacturing capabilities, or legal counsel, we know who to call — and we know how to build the right team around your program.
The Right Support at Every Stage of Development
We don’t do referral lists. The partners below are part of a deliberate ecosystem Facet has assembled over years of working at the front lines of novel drug, biologic, and device development.
Click on each company to learn more.
Cannovation is a U.S. based global clinical research organization (CRO) consulting firm that offers full-service preclinical/clinical research and commercialization services.
Cannovation is the first to partner with biopharmaceutical companies, universities, centers of excellence, and government agencies to bring innovative prescription and non-prescription therapeutics to market.
Cannovation provides turn-key consulting services to clients who research and develop of all therapeutics including non-traditional cannabinoid and psychedelic based drugs.
Lexitas is a premier clinical research organization dedicated exclusively to ophthalmology since 2011. With unmatched expertise and precision in ophthalmic research, we deliver tailored approaches, rigorous quality standards, and unwavering commitment to operational success. Our team of experts, including ophthalmologists, optometrists, and clinical operations specialists, brings extensive medical, scientific, regulatory, and operational knowledge across all ophthalmology subspecialties. With a deep understanding of patient treatment pathways, provider and research networks, and market opportunities, Lexitas provides customized solutions that support your needs at every stage of development.
TheranosticTrials.org is the premier global hub advancing cancer Theranostics by connecting every link in the Theranostic Trials Ecosystem. From discovery and development to isotope production, clinical trial operations, radioactive courier logistics, equipment and dosimetry, specialized staffing, capital investment, regulatory agencies, and cancer centers, we bring the field together to make it work in the real world. We expand awareness, showcase capabilities, and create networking opportunities that foster collaboration and accelerate impact. The site provides clear education and a comprehensive directory of cancer clinical trials, along with resources on key radioligand therapy (RLT) components such as isotopes and targets. Our mission is simple: work together to improve the lives of cancer patients worldwide.
Tranquil’s ultimate goal is excellence in the clinical trial process and bringing trustworthy products to patients.
Tranquil Clinical Research was created to ensure that the entire clinical trial, device, and drug development process is conducted with ethics and the patient in mind first and always. The business model ensures a clients drug, device or investigational product in the clinical trial is adherent to the highest level of quality and integrity in the services we provide.
Trialwise was founded by Beth Brinsdon in 1999 to specialize in the early phases of drug development.
During her two decades in the pharmaceutical industry, Beth observed that start-up and small-to-midsize biotech companies require a high level of personalized service, a level best provided by a small team of professionals working in a collaborative and flexible environment.
Contract Manufacturing
IDT Australia is an ASX listed Contract Development and Manufacturing Organisation (CDMO) company based in Melbourne with over 50 years of experience in pharmaceutical manufacturing. Our capabilities span the production of active pharmaceutical ingredients (APIs) through to finished dosage forms (FDFs), including oral (tablets, capsules, non-sterile liquids) and sterile injectable products. We support programs from pre-clinical development through to commercial-scale manufacturing. Our facilities are audited and accredited by the Australian Therapeutic Goods Administration (TGA), the U.S. Food and Drug Administration (FDA), and the Japanese Ministry of Health, Labour and Welfare. We also maintain regulatory standing in Europe and Canada through the Mutual Recognition Agreement. We also have Australian pesticides and Vetinary Medicines Authority (APVMA) accreditation.
Our parent company Pharmascience Inc. has developed strong roots in Canada, and is Quebec’s largest employer in the pharmaceutical field with over 1600 employees.
Royalmount CDMO has been operating out of the Candiac facility since 2014,
maintaining operations at this FDA-approved site. The facility’s capabilities have increased over time, progressing from development and manufacturing of small molecules to incorporating large molecules as well, such as Oligonucleotides, Monoclonal antibodies (mAbs) and Antibody-drug conjugates (ADCs).
Royalmount Labs external CRO business has become very successful, excelling in scientific excellence, customer service and on-time delivery. To accommodate the rapid growth, we continue to invest in the right staff, in the expansion and modernization of our laboratories, as well as in the latest technologies.
Document Management
Kivo is a software development firm with a tradition helping emerging life science companies, now with a new name. Kivo EDMS has been in the market for over eight years under the Gemstone brand by Facet Life Sciences. With new leadership and funding, we have built a modern submission management platform.
We strive to provide value-based solutions that fit the needs of early-stage life science organizations. Kivo complements its strong product offerings with exceptional customer support.
Ex-US Regulatory Affairs
Since its founding in 2000 by a small group of pharmaceutical R&D professionals with the vision to offer high-quality services for the development and registration of innovative drugs, Asphalion has evolved into a leading consultancy firm in regulatory affairs, life sciences services, marked by innovation and regulatory excellence.
GXP Audits
cGMP Validation was established in 1997 as a full service validation/compliance firm offering services for the pharmaceutical, bulk pharmaceutical, animal health, biotechnology, biologics, medical device and medical diagnostic industries.
cGMP Validation specializes in the preparation and execution of validation IQ/OQ/PQ protocols, compliance documentation for equipment, utilities, processes, laboratory instruments, and computer systems.
Legal
Troutman Pepper Locke helps clients solve complex legal challenges and achieve their business goals in an ever-changing global economy. Our goal in every matter is to ensure that your experience working with us is as exemplary as the results we help you obtain. To do that, we follow the core values and beliefs that have sustained and helped grow our firm for more than a century:
Medical Affairs
MedSurgPI, LLC provides Medical services for pharmaceutical, biotechnology, medical device and related technology companies and institutions in a cost effective manner. MedSurgPI was founded by and is led by two highly experienced clinician-executives whose combined backgrounds encompass medicine, surgery, technology, product commercialization and clinical development. We believe in product optimization, and preventing problems before you have to solve them.
Nonclinical CRO
Attentive Science is an FDA inspected, AAALAC accredited premier global leader, excelling in GLP and nonGLP in-vivo pharmacokinetics, toxicology, and safety pharmacology services. We serve the biotech, pharmaceutical, agrochemical and animal health industries, ensuring that data generated are accurate, complete, and verifiable paired with a personalized client service. Our team, with over two centuries of combined scientific experience, possesses extensive expertise in various test substances, test systems, routes of administration, and the overall conduct of preclinical (non-clinical) studies. This rich background ensures Attentive Science remains at the forefront of innovation, leveraging cutting-edge technologies and industry-leading methodologies to empower critical decision-making milestones. Partner with Attentive Science to fortify your quest for Healthier Outcomes globally.
Packaging and Printing Services
Nosco is a full-service packaging solutions provider serving over 400+ customers in the healthcare space. With more than 110 years of experience, Nosco brings together business resources and technical expertise to better understand packaging challenges and deliver customized solutions. The company focuses on service to help continuously improve efficiencies related to supply chain, cycle times, lean initiatives and product launches.
Nosco is a subsidiary of Holden Industries, Inc., and is 100% employee owned. The company employs 700+ employee owners, and specializes in printed packaging for the pharmaceutical, natural health, personal care and CPG markets with four core product lines: cartons, labels, inserts and flexible packaging.
Patent Support
Potomac Law is committed to innovation, excellence, and professionalism. Our value stems directly from the talent and commitment of our attorneys who practice law throughout the United States. Our attorneys have outstanding academic credentials and impressive professional experience, with an average of seventeen years at top national firms and/or in-house at major corporations. Clients recognize our attorneys’ skills and creative strategies, as well as their common sense and practical solutions.
Volpe Koenig is a full-service intellectual property law firm serving a diverse roster of U.S. and global clients across a varied mix of industries, technologies and business sectors. With almost 50 attorneys, agents and technical advisors, the firm provides strategic intellectual property counseling to protect valuable portfolios and assets. Volpe Koenig helps clients better understand the continually shifting IP legal landscape to provide our clients peace of mind knowing that their intellectual property assets are secure.
Regulatory Publishing
Red Nucleus is the premier provider of learning, performance, and process solutions for the life sciences industry. We work exclusively within the areas of pharmaceuticals, biosciences, and medical devices to ensure our team intimately understands your business, products, processes, and challenges. Our team is composed of more than 500 full-time employees whose commitment to creativity, quality, and on-time delivery is unrivaled in our space.
WAYS Pharmaceutical Services is an innovative team that helps biopharmaceutical organizations prepare and submit their research documents and supporting data to health authorities around the world.
Our team builds things. We build submissions. We build partnerships with our clients. We build trust.
Our track record speaks for itself. When you engage our team, we commit to your goals.
Our advisory, operational and training services are informed by our practical experience. We are constantly innovating and improving our processes to provide greater value to our clients.
CDISC/SEND
Veramed is a pioneering CRO redefining intelligent healthcare decision-making. As trusted industry specialists, Veramed’s global team provide next-level biometrics support to move the needle when it comes to delivering high quality, on-time deliverables across the drug development life cycle. Our skilled statisticians and programmers employ knowledge of statistical design, data visualization, automation, and workflow methodologies to facilitate everything from small-scale trials and global submissions through to launch and beyond. As a certified B Corp, Veramed tailors transparent and collaborative solutions to suit client needs, while staying true to a supportive culture that promotes a healthy work-life balance and employee happiness.
Awards & Recognition
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