Our Services
Research and Development in Pharmaceutical
Manufacturer and Supplier
MTS Laboratories has been providing high-purity specialty chemicals and intermediates to clients across Canada, China, and India. Additionally, we are actively serving the rest of the world (ROW) market, ensuring a widespread presence and impactful contribution.
Facilities
We are firmly dedicated to upholding secure and responsible practices concerning safety, health, and environmental protection, adhering rigorously to all pertinent regulations, international standards, and internal company protocols.
Our conviction lies in the fundamental belief that safeguarding human health and preserving the environment is not only essential but integral to the advancement of our business endeavors. With unwavering commitment, we pledge to conserve resources and ensure the well-being of our employees, customers, the environment, and the wider community.
- We have multi-purpose GMP compliance GL reactors capacity of 420 ltrs.
- Which is divided into 2 x 100 ltrs + 200 ltrs + 20 ltrs. Rotavapour.
Reactions
Impurities
- Contaminants
- Residues
- By-products
- Degradants
- Trace elements
Characterization
- Structure elucidation
- Chemical profiling
- Molecular weight determination
- Quantitative analysis
Quality Control
- Batch release testing
- Stability studies
- In-process controls
- Trend analysis
- Out-of-specification investigation
Detection and Analysis
- Chromatography
- Spectroscopy
- Mass spectrometry
- Nuclear magnetic resonance (NMR)
- Fourier-transform infrared spectroscopy (FTIR)
- High-performance liquid chromatography (HPLC)
Reactions
- Synthesis
- Hydrolysis
- Oxidation
- Reduction
- Isomerization
- Esterification
- Decarboxylation
- Cyclization
Risk Assessment and Mitigation
- Impurity profile
- Safety evaluation
- Toxicity assessment
- Risk management
- Control strategy
Compliance and Documentation
- Certificate of Analysis (CoA)
- Analytical method validation
- Batch record review
- Change control
Our Ability
Building Our Strength
Reaction Capabilities
- Methylation Reactions
- Amidations
- Nitrations
- Chlorination Reactions
- Hydrolysis Reactions
- Acetylation Reactions
- Condensation
- Oxidations
- Friedel Crafts Reactions
- Esterification Reactions
- Hydrogenation
- Catalytic Reduction Reactions
- Dry Ammonia Gas Reactions
Key Capabilities
- Competitiveness
- Offering excellent customer support through timely response and delivery
- Experienced and dedicated team of professionals through out the plant
- Contract manufacturing
- Our core values determine our strength, behavior and every interaction with customers. We give more priority to care, leadership and customer proximity than business success. Our values reflect our responsibility towards better future.
We are firmly dedicated to upholding secure and responsible practices concerning safety, health, and environmental protection, adhering rigorously to all pertinent regulations, international standards, and internal company protocols.
Our conviction lies in the fundamental belief that safeguarding human health and preserving the environment is not only essential but integral to the advancement of our business endeavors. With unwavering commitment, we pledge to conserve resources and ensure the well-being of our employees, customers, the environment, and the wider community.
- We have multi-purpose GMP compliance GL reactors capacity of 420 ltrs.
- Which is divided into 2 x 100 ltrs + 200 ltrs + 20 ltrs. Rotavapour.
One of the core principles of our research and development philosophy is to leverage our extensive expertise in chemistry to tackle novel challenges effectively.
We excel in providing innovative and efficient solutions across various projects, particularly in the following areas:
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Route and Process Development :
We specialize in improving problematic procedures or identifying optimal manufacturing routes for scalability. Our team's experience allows us to streamline processes, enhance efficiency, and ensure the highest quality standards in production. -
Route Design and Synthesis :
We are adept at designing routes and synthesizing novel analogues of lead molecules for optimization studies. Whether it's modifying existing compounds or creating entirely new ones, we possess the expertise to drive innovation and advance research in diverse fields.
Our commitment to excellence extends to our sourcing practices. We firmly believe in starting every product from basic raw materials. This approach not only aligns with our overarching vision but also empowers us to maintain control over critical raw materials. By controlling these essential components, we can ensure the quality and integrity of our products, thereby meeting the exacting standards of our customers.
In summary, our R&D philosophy revolves around harnessing our deep knowledge of chemistry to develop groundbreaking solutions, while also prioritizing quality and control through our meticulous approach to raw material sourcing and product development.
API & Intermediates
Exploring the Role of Active Pharmaceutical Ingredients (APIs) and Intermediates in Drug Development
The pharmaceutical industry is propelled by a nuanced interplay of various chemical entities, chief among them being Active Pharmaceutical Ingredients (APIs) and intermediates. These pivotal components serve as the bedrock upon which modern therapeutics are constructed, embodying the culmination of rigorous research, synthesis, and validation processes.
Active Pharmaceutical Ingredients (APIs)
Active Pharmaceutical Ingredients (APIs) and intermediates play pivotal roles in the development of pharmaceuticals, forming the backbone of modern medicine. These chemical compounds are the essential components responsible for the therapeutic effects of medications. Understanding their significance and the intricate processes involved in their development is crucial for advancing drug discovery and improving healthcare outcomes.
Intermediates
Intermediates, pivotal in pharmaceutical synthesis, bridge raw materials to active pharmaceutical ingredients (APIs). These transient compounds undergo precise chemical transformations, ensuring API potency and purity. Rigorous quality control and regulatory adherence govern their synthesis, fostering safe and efficacious drug development. Innovation drives optimization, from scalable manufacturing to sustainable processes, advancing pharmaceutical intermediates toward safer and more efficient drug production.
PROCESS DEVELOPMENT
Mts Laboratories has expertise in all phases of process development, from initial route exploration to enhancing and scaling up existing pathways. We've devised numerous alternative pathways for current molecules, offering cost-effective and scalable options for APIs, intricate intermediates, and novel chemical entities.
With a cumulative experience of over a century, we approach each project with a commitment to delivering fully integrated solutions, prioritizing quality, efficiency, and adaptability.
Our route exploration and comparative studies aim to identify more efficient synthetic pathways, reducing process steps, utilizing economical raw materials, and ensuring safety considerations.
Following this, our route familiarization studies pinpoint the most suitable pathway, considering delivery schedules and cost factors.
Our development activities span from laboratory experimentation to large-scale manufacturing, accompanied by comprehensive analysis and documentation for process validation. Mts Laboratories is your ideal partner for all your Process Development requirements.
Custom Synthesis
- Synthesis of novel chemical entities (NCE) and molecules.
- Innovative method development aimed at optimizing costs while prioritizing environmental sustainability.
- Design and creation of targeted analogue libraries to amplify lead generation and optimization efforts.
- Synthesis of reference compounds, metabolites, and impurity markers to ensure quality standards.
- Customized method development and seamless technology transfer for organic molecule synthesis as per client specifications.