We specialize in developing analytical methods — accurately, quickly and in full compliance with international standards.
Analytical Chemistry at the Service of the Pharmaceutical Industry
Q&Q Analysis Pharma
Q&Q Analysis Pharma supports pharmaceutical companies, contract manufacturers and biotech startups in the most critical stage before production: the creation of a method that works, reliably, from the first time.
WHY Q&Q Analysis Pharma?
Our Experience at Your Service

16+ Years of Experience
Experience in analytical chemistry and quality control

6 Cutting-Edge Analytical Technologies
HPLC, GC, LC-MS/MS, GC-MS/MS, ICP & ICP MS

5 International Compliance Standards
Compliance with ICH, Ph.Eur., USP, FDA, EMA
OUR SERVICES
Analytical Chemistry Services
We provide a comprehensive range of analytical services that cover all the needs of the pharmaceutical industry, from research and development to production and quality control.
Development of Analytical Methods
The development of reliable analytical methods is the cornerstone of quality control in the pharmaceutical industry. At Q&Q Analysis Pharma Laboratories we design and develop customized analytical methods, tailored to the specific requirements of each product, ensuring accuracy and compliance with international regulatory requirements.
Leveraging cutting-edge technology and drawing on 16 years of experience, we develop methods that are reliable, cost-effective, and suitable for transportation in manufacturing environments. We undertake the design and optimization of customized analytical methods using HPLC, GC, LC-MS/MS, GC-MS/MS, ICP, and ICP-MS for pharmaceuticals, raw materials, and finished products.
Key Points:
- Development of chromatographic methods (HPLC, GC, LC-MS/MS, GC-MS/MS)
- Spectroscopic & elemental determination (UV-Vis, ICP-MS)
- Quantification of active substances and impurities (related substances)
- Method optimization for smooth transfer to production
- Full documentation according to ICH, Ph.Eur., USP
WHO WE SERVE
We work with companies across the spectrum of the pharmaceutical industry
Pharmaceutical Companies
Support of R&D departments in the development of analytical methods for active substances, excipients and excipients, as well as in the adaptation of existing methods.
Indicatively, we undertake:
- Development of a method for a new active substance
- Method revision due to raw material change
- Sensitivity/Detection Limit Improvement
Contract Manufacturers
We develop analytical methods designed to integrate seamlessly into your existing production lines, without requiring costly equipment adjustments. Our goal is a method that works properly with transportation.
Indicatively, we undertake:
- Method development
- Method adaptation to new equipment
- Troubleshooting an existing method
Biotech Startups
An emerging biotech company rarely has its own, fully staffed analytical development department — and often doesn’t have the luxury of time or budget that an established pharmaceutical does. Q&Q Analysis Pharma acts as your external method development department, tailored to your own pace: we accompany you from the first product prototype to the stage when the method is ready to back up your file to regulator.
Indicatively, we undertake:
- Method development from scratch, even when the product is at an early stage
- Adjusting the method as the product progresses to subsequent stages of development
- Documentation of the method in the format required for regulatory submission
EQUIPMENT & CAPABILITIES
The most modern technological infrastructure
Our laboratories are equipped with state-of-the-art technology, through continuous and uninterrupted investments in new technologies. The available technological equipment and instrumental analysis instruments are constantly expanding, as the range of our services is expanding.
Equipment:
- HPLC – DAD, RI, FLD
- GC – ECD, NPD, FID
- LC-MS/MS
- GC-MS/MS
- UV-Vis
- ICP-MS
The equipment mentioned above is indicative.
Please contact us for more information

