Training

by | May 16, 2022 | Uncategorized

TRAINING These types of training methods do not make a full list, but they are the general methods that might be divided into sub-categories. As such, each is worth exploring and considering when an organization or trainer wishes to properly prepare an individual or a...

Process Validation

by | May 16, 2022 | Uncategorized

PROCESS VALIDATION GMP validation is an element of quality assurance program for a pharmaceutical/biotech product or process. To ensure that the products are absolutely fit for intended use, the company has to demonstrate in a documented form that the processes,...

Analytical Method Validation

by | May 16, 2022 | Uncategorized

METHOD VALIDATION We use comprehensive and fit-for-purpose procedures for the transfer, validation or even development from scratch of pre-qualified, pharmacopeia compendial and in-house methods in line with our client’s requirements and according to ICH, EMA,...

Laboratory Equipment Qualification

by | May 16, 2022 | Uncategorized

EQUIPMENT QUALIFICATION Neutron IQ/OQ documentation was founded on the following documentation tree, starting with the first module, the Master Document (MD), followed by the Installation Qualification (IQ) and finally the Operational Qualification (OQ). Master...

Laboratory equipment calibration

by | May 16, 2022 | Uncategorized

EQUIPMENT CALIBRATION Calibration in Pharmaceutical ApplicationsRegular calibration of instruments is commonplace for process manufacturers. But in the Pharmaceutical industry particularly, where instrument accuracy is critical to product quality and safety, strict...

Service Request

by | May 16, 2022 | Uncategorized

Service Request Service Request Form Request Date MM slash DD slash YYYY Request NOContact Company Address ChargeEmail* PhoneFaxNoteTurnaround Time ( Business Days ) Normal 10 days Rush 5 days Rush 3 days Rush 1 days Regulatory Requirements ISO 17025Traceability...