SUPERA QUALITY Ltd offers the possibility of internal education.
We design, develop and adjust the internal education to the specific needs of your company, institution or laboratory.
The goals of education, themes and duration are agreed with you in order to meet the best your specific needs.

All our seminars are combination of lectures and workshops where appropriate "case studies" are resolving. In agreement with you we check the effectiveness of performed education by testing.
Upon completion of the education we issue certificates/confirmations to participants so they can confirm the familiarity with certain topics during regulatory inspections or audits performed by certification or accreditation bodies.

The advantages of internal seminars

• Seminar goals and themes are adjusted to your specific needs
• Lower fee cost - smaller investment per seminar attendant
• Additional cost saving such as costs of transportation, accommodation and daily allowance
• Time and duration are adjusted to your needs 

List of selected internal education

• Good Manufacturing Practice (GMP) in production, storage and distribution of drugs

• Effective GMP audit and self inspection

• Education for internal ISO auditors - preparing for audit, audit

performance, non-compliances/deviations assessment, corrective and

preventive actions (CA/PA) proposing, reports drafting, monitoring the

system effectiveness

• Good practice in the laboratory - laboratory equipment qualification,

analytical methods validation, reagents preparation and storage, sampling,

standards managing and standardization, washing of laboratory dishes,

calibration of laboratory balances, pH meters and other measuring equipment

calibration, laboratory log book running, managing “out of specifications”

results (OS)

• Preparing and managing the successful regulatory inspection

• Good Documentation Practice - document management, production of guides,

general and work instructions, records management, preservation, archiving

• Preparation of Module III CTD of registration dossier - experiences from

practice

• Generic drug development – experiences from practice

• What an analyst should know about statistics

• Statistical Process Control

• What when the basic statistics is not enough

• Education on the requirements of ISO standards (ISO 9001:2008, ISO

14001:2004, ISO 22000:2006, ISO 17025:2007, ISO 13485:2003, ISO 15378:2006,

ISO 15189:2003)