BioPharma Services Inc. | Global CRO | Drug Development

Time 2021-09-22 19:18:13

Web Name: BioPharma Services Inc. | Global CRO | Drug Development

WebSite: http://www.biopharmaservices.ca

ID:197423

Keywords:

Inc,Services,BioPharma,

Description:

Think Research Corporation Closes Acquisition of BioPharma Services Inc.Toronto, ON, September 13, 2021 – Think Research Corporation today announced that it has closed its previously announced acquisition of all of the issued and outstanding shares of BioPharma Services Inc.Read the Press ReleaseVolunteersGetting a new drug onto the market is a process that can take many years. BioPharma Services helps companies ensure that drugs that are being developed are safe and effective. Take a look at our Frequently Asked Questions and other volunteer pages to learn more about how you can become involved by participating in a Clinical Trial.Visit our Volunteer HomeSponsorsLed by an expert panel of experienced Medical Physicians and Research Scientists, BioPharma has built a full suite of clinical trial solutions from Phase I to BE/BA services to assist our clients’ clinical drug development programs.                                                                                                                                                                                                     The BioPharma BenefitsWe Bring Pharmaceutical Products To MarketThe team at BioPharma Services is dedicated to bringing novel therapies to the market through high quality medical research.  Founded by the vision of two surgeons dedicated to advancing medical science and improving the life and quality of their patients, we brought life to BioPharma. It is with this same culture and brand of excellence that we welcome our clients.Click here to read our response to COVID-19. OurServicesAlong with our core clinical competency of flawless execution of Phase I, BE/BA and Human Abuse Potential studies, complementary support services are available to align with our clients’ clinical trial needs.As a full-service contract research organization, our service offering includes: Scientific, Medical and Regulatory Affairs, Bioanalysis, Data Management, Biometrics (CDISC compliant data standards), Medical Writing and long-term archiving of study documents.Our ServicesWhyBioPharmaAt BioPharma, we appreciate the dynamic and complex regulatory landscape that governs the drug approval process. Let’s work together to combine our knowledge, expertise, and know-how to navigate our way through the clinical development process and bring first-in-world and affordable medicines to every individual patient in need. With competence and compassion, we as a contract research organization, aim to earn the trust and respect of our global clients, employees, and patients.Why BioPharma?Quality andGovernanceIn this highly regulated industry that is governed by the international quality standards of GCP and GLP, it is paramount that our processes, quality and governance never falters. With strong adherence to the principles set forth by the ICH, BioPharma’s unwavering commitment to CRO research quality and safety standards is supported by our history of regulatory inspections that spans across markets. This includes routine regulatory inspections by the US FDA, UK MHRA, ANSM, DKMA, ANVISA and Health Canada and a GLP certification by the SCC.Quality and GovernanceClinical Trial ServicesState of the art facilities. World class leaders. Innovative scientific expertiseSupport ServicesTo ensure the successful submission of every trial, BioPharma offers a full suite of Support Services.View All Services SupportClinical Trial ServicesState of the art facilities. World class leaders. Innovative scientific expertise.Phase 1 2aWe collaborate with global pharmaceutical companies, making sure their program needs for early phase drug development are more than satisfied. BioPharma conducts Phase 1 clinical trials across a wide variety of therapeutic areas.Phase 1 2a ➞BioanalysisDelivering high quality, accurate and innovative solutions to support the drug development programs of our clients.Bioanalysis ➞Human Abuse PotentialBioPharma has amassed extensive experience in the conduct of clinical studies in opioids, narcotics and cannabinoid products. These studies help drug developers understand their product’s potential risk for abuse before seeking regulatory approval.Human Abuse Potential ➞BioequivalenceBioPharma has built a brand of excellence in the conduct of Bioequivalence (BE) and Bioavailability (BA) studies to support both generic and hybrid drug filings and 505(b)(2) New Drug Applications.Bioequivalence Bioavailability ➞Support ServicesState of the art facilities. World class leaders. Innovative scientific expertiseData ManagementEfficient, cost-effective services in a timely, expeditious manner packaged to meet the current regulatory and industry standards.Learn More ➞Medical WritingOur Medical Writing team ensures clear communication between subjects, sites, sponsors and regulatory agencies.Learn More ➞Biometrics/CDISCWith CDISC standards in mind right from data collection, BioPharma offers a suite of biostatistical services.Learn More ➞Scientific AffairsOur in-house experts have experience over a diverse range of clinical drug development programs for multiple therapeutic areas.Learn More ➞PharmacokineticsUnder the leadership of Chief Scientific Officer, Dr. John Oldenhof, the PK team have generated thousands of study designs to support drug submissions to multiple regulatory markets.Learn More ➞RecruitmentA fundamental element of success for any clinical trial is subject recruitment. Our extensive database of engaged healthy volunteers includes special populations.Learn More ➞Our PeopleTwo surgeons dedicated to advancing clinical science to improve patient outcomes founded BioPharma over 15 years ago. Today, our expanded team of multidisciplinary experts works together, building on this entrepreneurial foundation with common goals and values. We aim to exceed your expectations with our proactive approach and “can do” attitude.Welcome to BioPharma! We look forward to working with you.Learn MoreOur ClinicsWith two state-of-the-art clinical facilities with a total combined 300-bed capacity in Toronto, Ontario and St. Louis, Missouri, BioPharma has conducted approximately  2,500 bioequivalence and Phase I clinical trials and counting. We have experience conducting Phase I trials across a wide range of therapeutic areas, including neurology, cardiology, immunotherapies and infectious diseases.Learn MoreOur LabsLed by experts with over 20 years of expertise, our Bioanalytical Lab in Toronto is equipped with the latest LC/MC/MS platforms [JL2] to meet the demand for detecting increasingly lower amounts of drugs in biological samples. We develop novel assays and extraction methods that deliver consistent, accurate results on expedited turnaround times.Learn MoreRecruitmentA fundamental element of success for any clinical trial is subject recruitment. Our extensive database of engaged healthy volunteers includes special populations.CDISC Data StandardsCDISC data standards are becoming standard for all phases of clinical drug development and submissions to the FDA. We have the latest Biometrics Technology to ensure the successful submission of your application.505(b)(2) NDAThis FDA New Drug Application can be an effective regulatory pathway for new products with well-understood active ingredients. Let us guide you through the process.PharmacokineticsThe movement of a drug into, through, and out of the body is a fundamental component of the clinical drug development process. Our expert Pharmacokinetic Scientists have solutions for all drug programs.Schedule a Discovery Call TodayComplete the form to schedule a Discovery Call with one of our medical experts to learn how BioPharma Services can be your trusted clinical trial partner.By clicking “Accept All Cookies”, you agree to the storing of cookies on your device to enhance site navigation, analyze site usage, and assist in our marketing efforts. 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