Full project support — from concept to mass production
Мы обеспечиваем создание лекарственных средств и биологически активных добавок (БАД) под ключ – от разработки идеи до запуска серийного производства.
Our services
Consulting for startups in the field of pharmaceuticals and dietary supplement manufacturing
Development of a marketing plan, market analysis, patient flow and sales forecasting
Technological support and pharmaceutical development
Commercial production and pharmacovigilance
We will help you create a high-quality, effective, safe, and in-demand product within a reasonable timeframe and without unnecessary costs
Contact us to discuss your project and receive a detailed consultation
Trusted by
За время нашей работы сотрудники МБФ показали свой профессионализм. Компания обладает высококвалифицированными кадрами и современным оборудованием, а также не только следит за качеством выполняемой работы, но и учитывает пожелания заказчика. Рекомендуем МБФ…
По нашему опыту, компания МБФ является надёжным подрядчиком, на которого можно положиться. Работы выполняются в установленные сроки и на высоком качественном уровне.
Выражаем благодарность МБФ за продуктивное сотрудничество с АНО «Национальный научный центр Фармаконадзора» в области фармаконадзора. Хотим отметить ответственность и внимательность команды к задачам совместных проектов, что помогает обеспечить бесперебойну…
Frequently asked questions
Every project is unique, so we can only provide estimated timelines.
Launching a new dietary supplement brand on the market is quite quick. If the product is selected from our list of ready‑made and registered formulations, the customer only needs to approve the design and place an order for packaging materials. Such orders are completed within 2–3 months.
If a new composition is planned, its scientific and technological development will be required, as well as the state registration procedure. Such projects are usually implemented within a period of up to 6 months.
Запуск нового лекарственного препарата займет намного больше времени, нежели БАД. От появления идеи нового препарата до вывода его на рынок может пройти 5 - 10 лет: полная фармразработка формулы, доклинические исследования для проверки гипотезы и подтверждения механизма действия; затем - клинические исследования I и II фазы с участием добровольцев для всесторонней оценки безопасности и эффективности. Только после этого возможна регистрация лекарственного средства, которая сопровождается обязательным подтверждением контроля качества производственного процесса.
Launching a generic drug is simpler and faster, potentially taking about a year and a half. Since the pharmaceutical development phase and in-depth research have already been completed for the original drug, a generic version does not require extensive clinical or preclinical studies. Typically, a bioequivalence study is sufficient; in other words, it is necessary to demonstrate that the formulation matches that of the original (reference) drug.
Contract manufacturing involves producing items under your brand at our manufacturing facility. We can manage the entire project on a turnkey basis, or step in at any specific stage—whether that means developing a formula, selecting a product format, preparing documentation, or handling the technology transfer to move the production process to our facilities.
We can create an analogue of a product available on the market for you (a complete analogue in terms of components, or an alternative composition with the same effect). We can develop a complementary dietary supplement to complement your cosmetic line or in line with the logic of your service.
To start cooperation, please fill out the contact form on our website ([link to the form]) or reach out to us by phone at +7 (495) 721-20-58, +7 (916) 280-96-61 or via email: cp@mbpharma.ru.
Payment terms are always discussed individually and depend on many factors, including the volume of the batch, the availability of the required raw materials, the complexity and duration of preliminary work, and much more. In any case, we strive to be flexible and always take the customer’s interests into account.
We are ready to sign a non-disclosure agreement (NDA) with each client. If the contract includes any development work, all results will remain the property of the client.
Contact us
Filling out these documents will significantly speed up the processing of your request and the cost calculation
Download the documents and fill in the required information. If you have already submitted the form, you can send the documents and your request to our e-mail cp@mbpharma.ru including your contact details