[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text] In Greece QUALITECH wishes to fill in the Engineering/Construction & Qualification GAP the pharma, cosmetic and medical device (now food industry too) has, Out team consists of personnel with education and experience in pharma business not only as...

[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text] QUALITECH covers all the key areas to undertake effective cleaning of equipment and to validate the cleaning process: - Cleaning actions/chemistry involved, optimising cleaning processes and the use of cleaning agents - The design of equipment for ease of cleaning...

[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]Life cycle validation, verification, and testing (VV&T) is extremely important for the success of a simulation study. Current software VV&T techniques and current simulation model VV&T techniques are challenged and describe how they can all be applied throughout...

[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text] EU GMP regulations for clean rooms: 1. airborne particles with sizes ≥ 5.0 μm are differently counted and proposed between these two regulations. 2. FDA and EU GMP have different proposals on terminally sterilized and aseptically filled. products...

[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]There is always a strong ambiguous fight between consultants and customers upon producing a solid business plan and feasibility study, especially for new facilities or additional rooms, even when the investment is big enough to be considered above10Mio....

[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text] Benefits of Industry 4.0 [/vc_column_text][vc_column_text] Whether it’s Industry 4.0, Smart Industry or the Industrial Internet, there are ample benefits for manufacturers to transform the way they work. The essential goal of Industry 4.0 is to make manufacturing – and related industries...

[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text] SARS COV-19 is the virus name that is affecting worldwide so many countries and has made population go indoors for protection. Staying indoor protects mostly the old people, people we love and care about. But is it that...

[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text] As operations start coming back in reality, Qualitech Engineering offers a variety of Cleaning and Verification activities for Hospitals, Pharmaceuticals, Hotels and Public Buildings. Below the 7 Principles of Disinfection using DMAIC tools (Define-Measure-Analysis-Investigate-Control): 1. Assessment of Cleaning Procedures...

Qualitech proudly announces the first successful indoor air quality inspection for Hospitals and Hotels in April 2020. Using Inspection Protocols and Equipment for HVAC air sampling testing and cleaning, we offer a full spectrum service portfolio referring to Hospitals, Hotels and Industrial environments that want...

[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text] There is a lot of controversial articles we are reading on the net about FDA's decision to treat CBD products as potential drugs. All the implication show interest to support the transparent activities for Drug Master File and...