Business Programme
Day 1
Plenary session «Regulatory system and innovations. How to ensure the development of the innovative potential of the Russian pharmaceutical industry»
As a part of business programme, this plenary session, together with the heads of specialized associations, Russian pharmaceutical companies, and industry experts, will discuss the following topics:
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The effectiveness of government support measures at all stages of development life cycle of innovative medicines. Results of the work of the PharmMedInnovations venture fund.
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What types of innovations should Russian pharma concentrate on?
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Creating an ecosystem in Russia with multidisciplinary regulation and law enforcement in relation to R&D
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Legislative regulation of innovations in the pharmaceutical industry
Place: Pavilion 2, Hall 7, Main Hall
Language: Russian
Participation: free (with an electronic exhibition ticket)
Co-organizer: 
Plenary session «Regulatory system and innovations. How to ensure the development of the innovative potential of the Russian pharmaceutical industry»
Moderator:
Speakers:
Round table: Full cycle of API production. Road map
The full cycle of API production involves the creation of a full-fledged chain of manufacturers of all components: chemicals of varying complexity, from solvents to intermediates; the development of chemical engineering production, and training of personnel for all stages. Now this is all in its infancy. How far we have progressed along this path, what the results and prospects are and, most importantly, the timing - we will discuss these topics at the round table.
Place: Pavilion 2, Hall 7, Main Hall
Language: Russian
Participation: free (with an electronic exhibition ticket)
Partner: 
Full cycle of API production. Road map
Moderator:
Invited to event:
Seminars of participating companies
New technologies in clinical drug trials
Seminar by NPRC and IPMC of the Pirogov RNRMU
Programme:
«Experience in technological equipment of organizations conducting clinical trials»
A.E. Krasheninnikov, Doctor of Pharmaceutical Sciences, Head of the Department of Pharmacy, Institute of Pharmacy and Medicinal Chemistry, Russian National Research Medical University of Pirogova, General Director of the National Scientific Center for Pharmacovigilance
«Issues of pharmaceutical development and preclinical studies of drugs»
V.V. Negrebetsky, Professor of the Russian Academy of Sciences, Doctor of Chemical Sciences, Director of the Institute of Pharmacy and Medicinal Chemistry, Russian National Research Medical University of Pirogova
«Issues of technology for conducting bioequivalence, selection of a reference drug»
A. Kh. Sharafetdinov, Department for Regulation of Medicines and Medical Devices, Ministry of Health of the Russian Federation
«Practical experience in conducting research using high-performance liquid chromatography with tandem mass spectrometric detection (HPLC-MS/MS) produced in China» V.P. Ageev, Head of the Laboratory of Preclinical and Clinical Testing of Targeted Pharmaceuticals, Federal State Budgetary Educational Institution of Higher Education MSU named after N. P. Ogarev
Presentation of innovative projects in the field of quality of the finalists of the "GxP-PROFI 2023" contest
Place: Pavilion 2, Hall 8, Forum Hall
Language: Russian
Participation: free (with an electronic exhibition ticket)
Partner: 
Presentation of the 2023 GxP-PROFI finalists’ innovative projects in quality assurance
Мoderator:
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Seminars of participating companies
Lisure Science systems and solutions for industrial purification of vaccines, proteins and other biopharmaceuticals. Review of practical examples
Day 2
Round table: Mandatory labeling, import reduction, STM trend: the new reality of the dietary supplements market
Issues for discussion:
- Analysis of the situation on the dietary supplement market: trends, development factors, new opportunities
- The dietary supplement market in Russia: how production has transformed in order to meet customer requests
- Pitfalls when introducing new dietary supplements: real cases from practice
- Mandatory labeling of dietary supplements: roadmap and stages, how to avoid the most common mistakes, labeling in the context of contract manufacturing
- Innovative methods in the development of dietary supplements: factors for forming the quality of dietary supplements, safe additives = quality?
- Export and import potential. Bottlenecks in pharmaceutical logistics
- Raw materials, equipment, technologies. Is everything enough?
- Dietary supplement under private label (private brand). How much does it cost and what budget is needed for such a project.
Place: Pavilion 2, Hall 7, Main Hall
Language: Russian
Participation: free (with an electronic exhibition ticket)
Partner:
Round table: Mandatory labeling, import reduction, the trend for own brand: the new reality of the dietary supplements market
Moderators:
Speakers:
Round table: The Eastern vector in the technical support of pharmaceutical industries
Issues for discussion:
- Technological equipment West vs East
- Features of exporting equipment to China
- Logistics chains China-Russia. Problems and their solutions
- Localization of technological production
- Technology transfer in new realities
Place: Pavilion 2, Hall 7, Main Hall
Language: Russian
Participation: free (with an electronic exhibition ticket)
Partner:
The Eastern vector in the technical support of pharmaceutical industries
Moderator:
Speakers:
PHARMTECHPROM FORUM - 22 November
Dates: 22 - 23 November
Place: Pavilion 2, Hall 8, Forum Hall
Language: Russian
Participation: free (with an electronic exhibition ticket)
Session: Raw materials and pharmaceutical ingredients
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Session: Packaging equipment and materials for pharmaceutical production
Moderator:
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Day 3
Seminars of participating companies
High-tech laboratory and industrial equipment and consumables from Tailin Bioengineering
Seminar by REATORG
The seminar will be interesting for representatives of pharmaceutical production, quality control laboratories, R&D and microbiologists, as well as specialists working with such types of equipment as isolators, sterility and microbiological purity testing systems, glove integrity testers, total organic carbon (TOC) analyzers, generators hydrogen peroxide vapor.
AI based Bioengine serum-free culture media development for production of biopharmaceutical products
Seminar by Dia-M LLC
How to eliminate the risks of receiving low-quality secondary packaging at the original layout stage?
Seminar by PROMIS
For a pharmaceutical company, as for any brand holder, it is important that the colors in the design of secondary cardboard packaging are repeated from edition to edition. Transmitting color information to the printing industry in electronic format can guarantee accuracy.
Experts from the PROMIS company will talk about how instrumental control saves time and money for pharmaceutical manufacturers at the seminar «How to eliminate the risks of receiving low-quality secondary packaging at the the original layout stage?» The cases will be useful to heads of marketing and layout preparation departments, and heads of technology groups for packaging of pharmaceutical companies.
PHARMTECHPROM FORUM - 23 November
Place: Pavilion 2, Hall 8, Forum Hall
Language: Russian
Participation: free (with an electronic exhibition ticket)
Session: Technologies, equipment, auxiliary processes and products for pharmaceutical production. Part 1
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Session: Technologies, equipment, auxiliary processes and products for pharmaceutical production. Part 2
Moderator:
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