We use the following techniques
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 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.