Validations

NOVE OBAVIJESTI

Poštovani klijenti, obavještavamo Vas da od 21.04.2022., zbog povoljnije epidemiološke situacije te zbog ukidanja dosadašnjih ograničenja vezanih uz okupljanje većeg broja ljudi, a uz primjenu svih mjera opreza vezanih za sprječavanje širenja zaraze koronavirusom COVID-19, ponovno počinjemo s održavanjem kontaktnih seminara u prostorijama Supera Kvalitete, na adresi Gajeva 51- dvorišna zgrada, IV kat, Zagreb.

Osim kontaktnih seminara, i dalje će se neki seminari održavati online, a neki će biti kombinirani (polaznici će izabrati hoće li pratiti seminar onlline preko platforme Microsoft Teams ili nam se pridružiti  osobno u našoj učionici).

Molimo Vas da pogledate novi, izmijenjeni raspored svih seminara, a za dodatne informacije slobodno nas kontaktirajte. 

Kontaktni seminari SUPERA KVALITETA Sanja

SUPERA KVALITETA provides business consulting services for activities related to:

computer system validation, small application validation, cleaning validation, process validation, equipment qualification

 

Val rac sust 6Validation of information, laboratory and process systems and maintenance of computer systems in a validated state in compliance with applicable guidelines and guides: EU GMP Annex 11, ISPE GAMP 5, FDA 21 CFR Part 11 (for systems using electronic records and signatures) covers activities:

 

  • assistance in the preparation and / or review of validation documentation for all phases of the computer system life cycle (planning, specifications, development, installation qualification, operation qualification, performance qualification, "go-live")
  • assistance in producing the necessary procedures (SOP - Standard Operating Procedure)
  • risk analysis
  • audit of vendor 
  • performing education

 

Val rac sust 7We provide support for the creation and validation of small applications (Access, Excel, FileMaker) used in the GxP environment that must be validated.

 

 

Val rac sust 2We also provide support services for compliance of systems, computer systems and procedures with data integrity requirements in accordance with applicable guidelines.

 

 

 

Validacija ciscenja 1Cleaning validation - the purpose of cleaning validation is to confirm that the cleaning process is effective and to ensure that the medicinal product is safe by preventing cross-contamination.

Ceaning validation and maintenance of validated status in compliance with applicable Guidelines and Guides: EU GMP Vol 4. Part I and Part II, EU GMP Annex 15, PIC / S PI 006, APIC Guidance on aspects of cleaning validation in active pharmaceutical ingredient plants, FDA Guide to inspections validation of cleaning processes, ICH Guidelines, VICH Guidelines, covers activities:

  • assistance in preparation and / or review of validation documentation (validation master plan (VMP), cleaning validation protocol, cleaning validation report, descriptions of cleaning procedures - SOPs, work instructions, etc.)
  • pomoć u izradi matrice opreme proizvoda i grupiranju proizvoda
  • assistance in preparation of product equipment matrix and product grouping
  • assistance to set eligibility criteria and to calculate limits for the rest of the product
  • risk analysis
  • performing education

 

 Validacije validacija procesa

Process validation - documented evidence that a process run within set parameters can effectively and reproducibly produce a product that complies with predefined specifications and quality characteristics.

Process validation in accordance with applicable guidelines and guides: EU GMP Annex 15, EU GMP Chapter 5, EMA Guideline on Process Validation, FDA Guidance for Industry Process Validation, includes activities:

  

  • assistance in the preparation and / or review of validation documentation (validation master plan (VMP), validation protocol (validation plan), validation report)
  • risk analysis
  • consulting in the field of modern approaches to process development and validation: Quality by Design (QbD), Process Analytical Technology (PAT), Continued Process Verification
  • performing education

 

Kvalifikacija Picture1Equipment qualification - process that proves and documents that the equipment is functioning properly and that it really produces the expected results.

Equipment qualification in accordance with applicable guidelines and guides: EU GMP Vol 4. Part I and Part II, EU GMP Annex 15, EMA Guideline on Process Validation, PIC / S PI 006, WHO Annex 4 - Appendix 6, FDA Guidance for Industry Process Validation, includes activities:

  • assistance in the preparation and / or review of qualification documentation (User Requirements Specification (URS), Design Qualification - DQ), Factory Acceptance Testing (FAT), Site Acceptance Testing - SAT), Installation Qualification - IQ, Operational Qualification - OQ, Performance Qualification - PQ
  • risk analysis
  • performing education

 

We organize and perform in-house trainings in English language for computer system validation, small application validation, cleaning validation, process validation, equipment qualification and other similar topics.