Company MoCare Technologies s.r.ooperates in the healthcare and pharmaceutical industry. We specialize in the practical implementation of laws and regulatory rules into the production process throughout the company structure. Their fulfillment is a necessary requirement of state authorities and auditors of external partners.
For practical implementation, we use dozens of reliable experts with more than 10 years of experience who join together on the platform International GMP Network®. In this way, we take advantage of many years of experience and broad international contacts with relevant partners. We solve technical-engineering principles according to the recommended methodology of the worldwide organization of pharmaceutical engineers organized inprofessional societies ISPE® - International Society for Pharmaceutical Engineering.
We do not compromise on quality. We provide a comprehensive service from production support, process setup, staff training and motivation, implementation of the pharmaceutical quality system (PQS) and good manufacturing practice (GMP), ISO certification, legislative requirements for market introduction and we will recommend functional business models. Whether you are a foreign manufacturer or distributor who wants to enter the Czech market or a local manufacturer who needs support in production, certification and sales - WE ARE HERE FOR YOU!
Pharmaceutical production support
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Production of substances (API) and dosage forms
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Aseptic and sterile production
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Biotechnology and vaccine production
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Sterilization processes
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Clean spaces
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Pure Media (PW, WFI, CS)
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Management of maintenance processes
Quality systems
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Pharmaceutical Quality System (PQS)
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ISO for healthmeans
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Good Manufacturing Practice (GMP)
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Good Distribution Practice (GDP)
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Good Practice in Quality Control Laboratories
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Validation and transfer of analytical methods
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Stability
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Impurities
Specialized and professional topics
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Pharmaceutical toxicology
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Pharmaceutical microbiology
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Analytical Chemistry for QC
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Mapping pharmaceutical processes
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Risk management and assessment
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Strategies for Contamination Control
Project documentation, engineering support
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Concept studies and analyses
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Project management
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P&ID drawings for production, auxiliary and technical systems
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Project documentation
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URS, FS
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VMP, qualification protocols, documentation for monitoring critical parameters
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Commissioning of equipment and systems
Staff training
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Professional courses focused on pharmaceutical quality system issues
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Specific courses for individual GMP circuits
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Workshops on detailed GMP issues
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General corporate training
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Company training for specialists
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Individual training for specific problems
Ing. Jiří Moninec
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CEO GM PROJECT - Pharmaceutical and medical engineering
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TEVA Opava (GALENA s. p.) - Designing operations and equipment
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Development, development and new investment
Mgr. Marta Ugochukwu Monincová, Ph.D.
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Pharmaceutical quality system
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Microbiology
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Molecular Biology
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Biochemistry
Richard Ficek
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Project Management
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Sterile production
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Risk management and assessment
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Clean media systems
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Ventilation system
Ing. Kateřina Cáblová
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Project Management
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Concept study
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Project documentation
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Architectural and construction solutions
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Clean rooms
Ing. Ivana Monincová
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Concept study
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Project documentation
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Technological devices
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Clean media systems
Mgr. Lukáš Dvořák
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Pharmaceutical consultant (QC, PQS, QP)
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Qualified Person (QP)
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Management of Quality Control (QC) and Pharmaceutical Quality System PQS
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GMP expert for ČIA - Czech Institute for Accreditation
Uday Kumar Killi, Ph. D.
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Registered Pharmacologist and Toxicologist
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Assistant Professor
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Pharmaceutical Toxicologist
