Raw materials :
Pharmaceutical API, Vitamins, excipients, powder, solid, semi solid or liquid.
Bottles, caps, boxes, labels, tubes, aluminum foil or plastic etc.
Finished products :
Tablets, Capsules, Pouches, Suspensions, Creams, Lotions, Gels, Pastes, Shampoos and much more
We Perform the following analyzes according USP, Ph.Eur, FCC etc.
Amino acids Identification and determination
Heavy Metals Analysis
Minerals Identifications and assay
Pesticides Identifications and analysis
Residual solvents Identification and analysis
Total organic carbon (TOC)
Vitamins Identifications and assay
We use the following techniques
Using the following equipment and methods
HPLC Liquid Chromatography
GC Gas Chromatography
TLC thin layer chromatography
Atomic Absorption Spectrophotometry (AAS)
Research and developments
Our expertise in qualification. development and validation of analytical methods such as stability indicating methods according to ICH standards and other intrenationaly recognized methods are just a small part of the services Technikad offers.
You can be confident with our capable and comprehensive management of your products accelerated, initial and real time stability studies according to pre-approved protocols based on ICH or FDA or EU guidelines. Your samples are monitored and stored in qualified stability rooms for accelerated or long-term stability studies performing analysis at each required station, investigating any out of specification result and producing the final complete stability study report.
Technikad uses the services of a fully qualified and licensed microbiological laboratory accredited by Health Canada to perform microbiological analysis of samples, providing one stop service and is responsible for providing you competitive price and integrated certificate of analysis.
Technikad handles analysis and validation of the cleaning processes on different equipment surfaces and ensures the complete removal of contaminants by determining the limits permitted in the worst case
Technikad Analytics helps customers comply with good manufacturing practice and laboratory (GMP / GLP), writes the quality documents such as standard operating procedures (SOPs), change controls, reports, protocols, etc. Established specifications of analyzes of raw materials, packaging components and finished products according to the Health Canada standards and current pharmacopoeias
Possibility to save big on your analytical costs
You have a new project?
We take care of redaction of the new specifications of analysis for the raw materials, packaging components and finished products according the recommendations of clients, health Canada standards and current pharmacopoeia
Do you have old specification of analysis?
We cab also review and update the old specifications of analysis and offer the possibility to realize significant savings on analytical costs.