What are we doing?
ADDRESSŞenesenevler Bostancı, İstanbul
CONTACT US+90(549) 418 17 36
WRITE TO USinfo@fyconsultancy.com
What project would you like us to start with you today?
- Cost Saving Projects
- Rapid Test implementation for Microbiological Testings
- Quality Control Labs. Optimizations
- Software Development for Pharma/Medical Device Industry Consultancy
- Localization /Technology Transfer Projects
- Cleaning Validation Projects (with PDE Approach)
- Microbiological Saving Projects
- Computerized Systems Validation Projects
NITROSAMINE IMPURITY RISK EVALUATIONS WILL BE REQUIRED FOR ALL HUMAN MEDICINAL PRODUCTS – ARE YOU PREPARED?
If you are dealing with human medicinal products, you should perform a risk evaluation for all of your products.
The risk evaluations themselves do not need to be submitted but the outcome (risk identified or no risk identified) should be reported to competent authorities by
31 March 2021 for chemical medicines
1 July 2021 for biological medicines
Temporary and Permanent Staff Employment Services
25+ years of industry experience and a network that can be used by knowing many industry professionals personally, we can determine professionals to your open position based on the real needs of your company and your company culture.Read More
GAP Analyses and Consultancy
FY Consultancy also offers detailed remedial action plan and guidance on how it should be implemented, by determining individuals and timelines.Read More
We analyze all your GxP documents in parallel with your current workflows and cGMP requirements. We ensure that your documentation system consists of documents with the most optimal content and number, and that recurring and redundant documents are removed from the system.Read More