We commited to archieve comliance, ensure quality and protect your values.
We believe in creating partnerships with a purpose, dedicated to driving significant outcomes with measurable value. When you work with us, expect a collaboration of transparency, communication, and consistency.
Our people are coming from the pharmaceutical sector and have strong background in Chemistry and Chemical /Mechanical Engineering. Our experience with Greek and International companies has been a significant factor for Qualitech’s Team adaptation to difficult projects in difficult times. For the first time in Greece a company undertakes projects referring to Validation /Qualification of Equipment, Quality Assurance Projects, Pharmaceutical Engineering and Software Development/Validation. Our strong knowledge of regulations and experience on the field with International regulations and audits we perform and support, gives us the strategic advantage of combined activities that are always liable to legislation.
Ioannis has been working in the FMCG and Pharmaceutical Industry for more than 10 years in positions of responsibility and has a strong chemical engineering background with process and analytical skills throughout the daily contact with every department of a modern pharmaceutical company. He has strong intellectual skills and takes up turn key projects and stays on top of them until they are delivered. His handful project experience gives the customers the opportunity to be agile and functional before start up and audit day.
Engineering Project Management and at the same time Construction Supervision ensure the unparalleled advantage of progress within time schedule.
Qualification & Validation Activities cover all companies and production sites and are delivered with integrity, accuracy and consistency.
Ensuring continuous compliance through personnel training and project handover. Our consultants deal with tough decisions, thus making them first of choice.
Our consulting and validation expertize, assure high FDA and MHRA as well as EU GMP standards, tailoring all solutions to each customer, bringing on technology and regulation into harmony.
Our partners operate around the world delivering on time precise and integer GxP audits for 2nd and 3rd parties. We assure you stay up to date and get the most out of the inspections.
We run protocols with our customers’ approval for more than 100 pharmaceuticals and other industries on Clean Rooms, HVAC Engineering and Maintenance, Machine Qualification Protocols and Facility Maintenance Projects. Our services combine experience and efficient regulatory compliance.
We support Food companies to conform with Food Safety and GMP standards, ISO2200, IFS, BRC, FDA and HACCP development, as well to establish an industrial hygiene design We carry out internal inspections, gap analysis, environmental monitoring, auditing and improvement plan projects.
Scientific and regulatory capability for nutraceuticals and food innovative products. Sustainable raw & packaging material sourcing. Market research and business plan execution. Development of new formulations and ensuring for the labelling compliance.
Our Expert Team in Disinfection and Decontamination Control has undertaken projects under the COVID -19 threat for Hospitals, Public Buildings and Hotels.
Qualitech Engineering has GxP engineered and Qualified the 1st N. Macedonian Site to receive GMP Audit Certification.
Qualitech has been acting as GMP consultant for all Greek Herbal Medicine Projects asserting legislation touches down to manufacturing.
Experienced consultants with multinational presence, are on top of ongoing domestic and international projects in pharmaceutical sector.
Since 2018 Qualitech Engineering Team has been involved in numerous projects in engineering and validation of modern facilities in Greece and Europe.
Qualitech’s Computer Systems skills and know-how delivered an ERP validation project in no time. We passed all audits!
Anna from Sterile Manufacturing in Greece
Qualitech has state-of-the-art equipment for Clean Room Validation and along with up to date QMS documents, they performed well during our FDA inspection.
Argus from Biotech Italy
Ioannis and his team is well trained and maintain a good regulatory compliance status through continuous training process.
George from OSD Production in Greece