MedStartUp
Phone: +7 705 170 8825; +7 705 170 8879
E-mail: info@medstartup.asia
MedStartUp is a full-service Contract Research Organization (CRO), Clinical Research Center, and Bioequivalence Center headquartered in Almaty, Kazakhstan. As a subsidiary of ConsultAsia, a well-established regulatory and pharmaceutical consulting company specializing in medicinal product registration, regulatory affairs, market authorization, and market access across Kazakhstan and the Eurasian Economic Union (EAEU), MedStartUp delivers fully integrated solutions that bridge regulatory expertise with clinical research excellence.
Our mission is to simplify and accelerate the journey from pharmaceutical development to successful commercialization. By combining scientific knowledge, regulatory intelligence, and operational excellence, we help pharmaceutical, biotechnology, and medical device companies navigate complex regulatory environments, conduct high-quality clinical research, and bring innovative healthcare products to patients efficiently and compliantly.
Unlike traditional CROs that focus solely on clinical operations, MedStartUp offers an integrated development platform where regulatory strategy, clinical research, bioequivalence, and commercialization support are managed within a single organization. This approach minimizes development timelines, reduces operational complexity, and provides sponsors with a single strategic partner throughout the product lifecycle.
Our services cover every stage of pharmaceutical development, including regulatory strategy, product registration, Phase I clinical trials, Bioequivalence (BE) studies, Bioavailability (BA) studies, Therapeutic Equivalence studies, clinical project management, clinical monitoring, site management, subject recruitment, pharmacovigilance, medical writing, quality management, ethics committee coordination, regulatory submissions, and post-registration support.
Through ConsultAsia's regulatory expertise and MedStartUp's clinical capabilities, sponsors benefit from comprehensive support for medicinal product registration, lifecycle management, dossier preparation (CTD/eCTD), variation management, market authorization, pricing and reimbursement consulting, and regulatory compliance within Kazakhstan and the EAEU region.
Our multidisciplinary team consists of experienced physicians, principal investigators, clinical research professionals, pharmacists, regulatory affairs specialists, bioanalytical experts, quality assurance professionals, and project managers dedicated to delivering scientifically sound, ethically conducted, and regulatory-compliant clinical research. Every project is managed according to ICH-GCP and applicable international quality standards with a strong focus on patient safety, data integrity, operational efficiency, and scientific excellence.
Strategically located in Kazakhstan, MedStartUp provides sponsors with efficient access to one of the fastest-growing clinical research regions connecting Europe, Central Asia, and the Eurasian Economic Union. Our regional expertise, combined with international quality standards, enables sponsors to conduct studies efficiently while meeting global regulatory expectations.
Whether supporting multinational pharmaceutical companies, biotechnology innovators, generic manufacturers, medical device developers, or emerging life science companies, MedStartUp is committed to building long-term partnerships based on quality, transparency, reliability, and measurable results.
Core Services
- Full-Service Contract Research Organization (CRO)
- Phase I Clinical Trials
- Bioequivalence (BE) Studies
- Bioavailability (BA) Studies
- Therapeutic Equivalence Studies
- Clinical Trial Management
- Clinical Monitoring
- Site Management
- Subject Recruitment
- Medical Monitoring
- Regulatory Affairs
- Pharmaceutical Registration
- CTD & eCTD Dossier Preparation
- EAEU Regulatory Consulting
- Market Authorization Support
- Pharmacovigilance
- Medical Writing
- Ethics Committee & Regulatory Submissions
- Quality Assurance & GCP Compliance
- Post-Marketing Regulatory Support
For detailed contact information visit location pages below.