Innovative R&D,
Reliable Analysis,
Sustainable Quality!
WMINOLAB Innovation Laboratory
Analytical Solution Partner
We provide analytical solutions aligned with sustainable quality standards through innovative R&D studies that enhance product quality and reliability in pharmaceutical drug analysis.

ISO 17025:2017 accredited in Extractables & Leachables, Nitrosamines,
and Elemental Impurities
First and unique laboratory in Türkiye analysis.
We provide reliable and precise analytical services in accordance with international standards as the first and unique ISO 17025:2017 accredited laboratory in Türkiye.
ISO 17025
ISO 50001
ISO 13485
ISO 27001
ISO 14001
ISO 9001
GMP
ISO 17025
ISO 50001
ISO 13485
ISO 27001
ISO 14001
ISO 9001
GMP
TÜRKAK
GMP
ISO 9001
ISO 14001
ISO 27001
ISO 13485
ISO 50001
High-Tech Analytical Laboratory Services
Method Development
Method development is a critical first step in ensuring the reliable detection of routine sample analyses.
Effective method development not only optimizes laboratory resources but also ensures consistent performance and efficient global transfer of the method.
We have strong expertise in developing analytical methods for a wide range of techniques, utilizing advanced technologies such as LC/Q-TOF, LC-MS/MS, GC-MS, and ICP-MS.
Method Validation
WMINOLAB conducts method validation studies in GMP certificated laboratories according to ICH, FDA, USP, EP, and BP guidelines to ensure that analytical methods are suitable for their intended use.
Validation studies are carried out by considering critical parameters that may affect method performance.
WMINOLAB provides full or partial validations, re-validations, and method transfers across various analytical activities and final product specification verifications. All activities are comprehensively documented with protocols, procedures, and analytical reports reviewed by Quality Assurance.
Analytical Solutions
WMINOLAB offers a wide range of analytical services to support product release, development processes, and regulatory dossier requirements.
Our qualified experts, equipped with strong academic backgrounds and extensive R&D experience, take the time to thoroughly understand your analytical needs.
Our innovative perspective, state-of-art instruments, deep knowledge, and industry expertise enable us to meet your evolving product requirements as regulations continue to change.
We assess the quality, safety, and sustainability of your products in compliance with regulatory standards and performance criteria through comprehensive laboratory analyses.
We act as your solution partner to help bring your products to market quickly and cost-effectively.
Innovative R&D Studies
Extractables&Leachables
- Composition Analysis
- Product Safety
- Quality
Determination of Elemental Impurity
- Determination of impurities
- Product Safety
- Quality
In Vitro Performance Tests
In vitro performance tests scientifically verify the product design.
- Effective
- Product Safety
- Quality

WMINOLAB Laboratories
Mass Spectrometry Analysis Laboratory
Gas Chromatography Analysis Laboratory
Instrumental Analysis Laboratory
Microbiology Analysis Laboratory
Chemical/ Physical Analysis Laboratory
Mass Spectrometry Analysis Laboratory
Advanced analytical solutions are offered with high precision in our laboratory equipped with state-of-art devices that allow the identification of chemical components, determination of purity degrees and detailed examination of the molecular structure of substances
Gas Chromatography Analysis Laboratory
Contributing for product reliability by decomposing, analyzing and determining components that can become gases or vapors, as well as detecting active ingredients and impurities of pharmaceutical products, stability tests and pharmacokinetic studies
Instrumental Analysis Laboratory
Critical analysis processes such as quality control, active substance and excipient, stability and specification tests are carried out in accordance with quality requirements in order to plan the correct licensing journey by guaranteeing the effectiveness and safety of pharmaceutical products
Microbiology Analysis Laboratory
Microbiological quality control tests are performed to determine the presence of pathogens and toxins in the treatments applied to patients. In order to prevent microbiological contamination of pharmaceutical products, the quality requirements for non-sterile and sterile products are met
Chemical/ Physical Analysis Laboratory
The studies are carried out to determine the chemical and physical properties of the sample by correctly defining in order to ensure quality assurance in production processes, to demonstrate the compliance of products with legal and industry standards
