Company profile
Contact details
WHO is Advanced?
We are a Team of international and Egyptian pharmaceutical industry experts for helping you to OPTIMIZE YOUR MANUFACTURING SITE according to latest cGMP & cGEP requirements and as per your specific needs.
We are a dedicated company specialized in training and consulting.
We could offer you a collection of training programs that covers most aspects of Good Manufacturing Practice and Quality Assurance in the field of Pharmaceutical industry.
ADVANCED, has staff with considerable experience in the manufacturing and quality management of pharmaceutical industry. Our workforce consists of international experts in topics such as quality managements, OOS investigation and quality control laboratories practices. This ensures that the training provided remains topical ..., addressing current issues and meeting the needs of those who attend.
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Why Advanced?
o Advanced are highly qualified persons with wide experience in pharmaceutical industries fields and updated regulations of WHO, FDA and EU covering all industrial branches (engineering, quality management and production,.)
o Advanced consultation covers different stages of pharmaceutical projects (design of manufacturing site, revision of layouts, revision of engineering drawings of all services. including (HVAC drawings, services pipe work and electrical single diagram in additional of any drawings related to industrial field), URS preparation for machines, services and systems, supplier evaluation, finishing specification, qualification & validation and revision of all documents and plans.
o Advanced provide in your site cGMP training for your staff, help your staff to build integrated quality system, preparing and review and update the documentation system including SOPs ,Master plans, protocols,.
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What can we do for you?
For under construction sites.....
o Creation of site layout and room book according to user requirements (URS) and cGMP requirements.
o Preparation of user requirements specification for machines, HVAC, water treatment and revision of engineering drawings of all services (HVAC drawings, services pipe work and electrical single diagram in additional of any drawings related to industrial field.
o Revision of supplier offers and optimizes your choice according to URS computability and quality standards.
o Projects management including planning, preparation and supervision of project time schedule... etc.
o Help you to optimize selection for the project consultants and contractors in difference fields related to project.
o Supervise qualification process (DQ, IQ, OQ and PQ) of building, machines and utilities.
o Technical visits to the site to ensure effective implementation of design.
For existing sites ....
o GMP training.
o By co-operation with Indian R&D Labs we can supply impurities and degradation products especially in case of impurities and degradation impurities which are not available with Pharmacopoeia or commercially. We support with the working standards complete characterization data with economic prices.
o Quality inspection of your site and help you to create preventative and corrective action for remarks.
o Advanced perform site upgrading to match cGMP guide lines and regulations as WHO, FDA and EU.
o Engineering supports include infrastructure, production lines, Services equipments and HVAC system.
o Engineering planning including preparation and supervision of calibration plans, Major and minor maintenance plans, Maintenance training. (Covering production lines, Services equipments and plants, HVAC system.).
o Trouble shooting, preventive and corrective action, problem solving and upgrading of factory production lines, services and HVAC equipments.
o Validation training with supervising practical execution.
o Review and update documentation system.
o Update production area as per latest requirements.
o Helps in site preparation for national and international audits. Read more
We are a Team of international and Egyptian pharmaceutical industry experts for helping you to OPTIMIZE YOUR MANUFACTURING SITE according to latest cGMP & cGEP requirements and as per your specific needs.
We are a dedicated company specialized in training and consulting.
We could offer you a collection of training programs that covers most aspects of Good Manufacturing Practice and Quality Assurance in the field of Pharmaceutical industry.
ADVANCED, has staff with considerable experience in the manufacturing and quality management of pharmaceutical industry. Our workforce consists of international experts in topics such as quality managements, OOS investigation and quality control laboratories practices. This ensures that the training provided remains topical ..., addressing current issues and meeting the needs of those who attend.
-------------------------------------------------------------------
Why Advanced?
o Advanced are highly qualified persons with wide experience in pharmaceutical industries fields and updated regulations of WHO, FDA and EU covering all industrial branches (engineering, quality management and production,.)
o Advanced consultation covers different stages of pharmaceutical projects (design of manufacturing site, revision of layouts, revision of engineering drawings of all services. including (HVAC drawings, services pipe work and electrical single diagram in additional of any drawings related to industrial field), URS preparation for machines, services and systems, supplier evaluation, finishing specification, qualification & validation and revision of all documents and plans.
o Advanced provide in your site cGMP training for your staff, help your staff to build integrated quality system, preparing and review and update the documentation system including SOPs ,Master plans, protocols,.
-------------------------------------------------------------------
What can we do for you?
For under construction sites.....
o Creation of site layout and room book according to user requirements (URS) and cGMP requirements.
o Preparation of user requirements specification for machines, HVAC, water treatment and revision of engineering drawings of all services (HVAC drawings, services pipe work and electrical single diagram in additional of any drawings related to industrial field.
o Revision of supplier offers and optimizes your choice according to URS computability and quality standards.
o Projects management including planning, preparation and supervision of project time schedule... etc.
o Help you to optimize selection for the project consultants and contractors in difference fields related to project.
o Supervise qualification process (DQ, IQ, OQ and PQ) of building, machines and utilities.
o Technical visits to the site to ensure effective implementation of design.
For existing sites ....
o GMP training.
o By co-operation with Indian R&D Labs we can supply impurities and degradation products especially in case of impurities and degradation impurities which are not available with Pharmacopoeia or commercially. We support with the working standards complete characterization data with economic prices.
o Quality inspection of your site and help you to create preventative and corrective action for remarks.
o Advanced perform site upgrading to match cGMP guide lines and regulations as WHO, FDA and EU.
o Engineering supports include infrastructure, production lines, Services equipments and HVAC system.
o Engineering planning including preparation and supervision of calibration plans, Major and minor maintenance plans, Maintenance training. (Covering production lines, Services equipments and plants, HVAC system.).
o Trouble shooting, preventive and corrective action, problem solving and upgrading of factory production lines, services and HVAC equipments.
o Validation training with supervising practical execution.
o Review and update documentation system.
o Update production area as per latest requirements.
o Helps in site preparation for national and international audits. Read more
Other Products
- GMP Consulting
- GMP Education & Training