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LGM Pharma - CDMO/CMO
LGM is the Ttusted Full Turnkey CDMO Partner, providing an integrated suite of solutions from initial formulation development to ongoing commercial manufacturing.With three strategically located US based manufacturing facilities in California, Colorado, and Texas, we offer a wide rage of dosage forms with regulatory CMC support.
To properly serve our clients’ unique needs, we reinvented the typical CDMO internal structure through the lens of Quality by Design (QbD). As a result, we are uniquely integrated; for example, our regulatory submissions team is embedded within our R&D team, ensuring that every decision we make on behalf of your project will help—not hinder—your FDA approval process.
United States
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Portfolio of over 2,000 APIs
Precise quality control
End-to-end global regulatory support
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Finished formulation / FDF
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Contact LGM Pharma for Contract Services Expertise
Connect with LGM Pharma, a leading pharmaceutical company from United States. They offer specialized CMO/CDMO - Contract (Development) Manufacturing Organizations, Analytical services, of which the services for CMO/CDMO include Tablets, Capsules, Topical formulation. Contact LGM Pharma for free and discover if they are the perfect partner for your pharmaceutical needs.
CMO/CDMO - Contract (Development) Manufacturing Organizations
CDMOs and CMOs are pivotal in the pharmaceutical and biotech industries, offering specialized services in drug development and manufacturing. They assist in scaling up production from laboratory to commercial quantities, while adhering to strict regulatory standards. These organizations play a crucial role in the efficient and cost-effective production of medical and pharmaceutical products, ensuring quality and compliance at every stage.
Pharmaoffer's category for Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) encompasses a wide range of specialized services crucial to the pharmaceutical and biotech sectors. These organizations, often referred to as pharmaceutical CDMOs or drug CMOs, are instrumental in advancing drug development and manufacturing processes.
Key Functions of CMOs/CDMOs:
Drug Development and Manufacturing Expertise: Offering comprehensive services in drug development, from initial research and development to full-scale manufacturing. This includes CDMO services and CMO manufacturing, ensuring a seamless transition from concept to market.
Scalability Solutions: Assisting in scaling production from laboratory to commercial scale, meeting the demands of various projects while maintaining quality and efficiency. This is where the expertise of a full-service CDMO becomes invaluable.
Regulatory Compliance and Quality Assurance: Ensuring adherence to strict regulatory standards such as FDA and EMA guidelines, and implementing rigorous quality control measures throughout the manufacturing process. This includes operating within GMP certified facilities to guarantee the highest standards of production.
Cost-Effective Production: Providing efficient and cost-effective solutions for the production of medical and pharmaceutical products, enabling companies to focus on innovation and marketing. CMO contract manufacturing plays a key role in this aspect.
End-to-End Service Provision: From concept to commercialization, CMOs/CDMOs offer a range of services including process optimization, formulation development, clinical trial material production, and commercial manufacturing. This comprehensive approach is often referred to as Contract Development Manufacturing.
Connect with Leading CMOs/CDMOs
Through Pharmaoffer, you can explore and connect with a comprehensive range of CMOs/CDMOs. Our platform offers access to organizations that play a vital role in the efficient, quality-assured, and compliant production of pharmaceutical and medical products, supporting the industry's growth and innovation. Whether you're looking for a CDMO partner, CDMO solutions, or contract manufacturers in pharma, Pharmaoffer is your gateway to the best in the industry.
Analytical services
Analytical Services in the pharmaceutical industry play a crucial role in drug development and quality assurance. Understand how Analytical Services, including methods like HPLC, GC-MS, and spectroscopy, play a critical role in drug development and quality control. Discover their significance in adhering to regulatory standards such as FDA and EMA guidelines. Uncover the impact of Analytical Services on the pharmaceutical industry through our comprehensive insights, aiding in informed decision-making.
Pharmaoffer's platform provides access to providers of contract Analytical Services, a fundamental aspect of the pharmaceutical industry. These services, encompassing Pharmaceutical Analytical Services and Bioanalytical Services, are integral to drug development and quality control, ensuring adherence to regulatory standards and the efficacy and safety of pharmaceutical products.
Key Aspects of Contract Analytical Services:
Advanced Analytical Techniques: Utilization of sophisticated methods such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography-Mass Spectrometry (GC-MS), and various spectroscopy techniques for accurate drug analysis. This is a cornerstone of services offered by analytical testing laboratories and Pharma Laboratories.
Regulatory Compliance: Ensuring that all analytical testing and processes meet the stringent guidelines set by regulatory bodies like the FDA and EMA. This includes GMP analytical testing, which is crucial for maintaining high standards in pharmaceutical analysis.
Quality Control and Assurance: Critical role in quality control and assurance, verifying the composition, purity, and potency of pharmaceutical products. Analytical Laboratory Services play a pivotal role in this process.
Support in Drug Development: Providing essential support in the drug development process, from early discovery through to clinical trials and commercialization. This includes chemical analytical services that are vital for comprehensive pharmaceutical research.
Informed Decision-Making: Aiding pharmaceutical companies in making informed decisions through comprehensive data and analysis provided by Pharmaceutical Analysis services.
Discover the Impact of Analytical Services
Through Pharmaoffer, you can explore and connect with specialized providers of contract Analytical Services. Our platform ensures access to services that are crucial for meeting the high standards of the pharmaceutical industry, supporting the entire lifecycle of drug development.
Finished formulation / FDF
Finished Formulation CMOs/CDMOs focus on the final stage of pharmaceutical product manufacturing, which involves blending and formulating active pharmaceutical ingredients (APIs) into finished dosage forms like tablets, capsules, liquid formulations, and injectables.
Pharmaoffer showcases a range of Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) that specialize in Finished Formulation. These organizations, key players in FDF (Finished Dosage Formulations) manufacturing, are essential in the pharmaceutical industry, focusing on the final stage of product manufacturing – blending and formulating APIs into finished dosage forms.
Key Services Provided by Finished Formulation CMOs/CDMOs:
Diverse Dosage Form Production: Expertise in creating a wide array of finished dosage forms, including tablets, capsules, oral liquids, powders, and more. This service is a critical aspect of FDF CDMO offerings.
High-Quality Formulation Development: Developing formulations that ensure efficacy, stability, and patient acceptability, adhering to precise pharmaceutical standards. This includes specialized formulation services and CDMO formulation development.
Advanced Manufacturing Processes: Utilizing state-of-the-art manufacturing processes and equipment to produce high-quality finished pharmaceutical products. This is a key component of CDMO products and contract formulation services.
Regulatory Compliance and Quality Assurance: Ensuring all products meet stringent regulatory standards, including compliance with FDA, EMA, and other regulatory bodies’ guidelines.
Customized Manufacturing Solutions: Offering tailored solutions to meet the unique needs of different pharmaceutical products, from small-scale batches to large-scale commercial production. This flexibility is essential in the realm of FDF manufacturing.
Connect with Expert Finished Formulation Providers
Through Pharmaoffer, you can explore and connect with CMOs/CDMOs that specialize in Finished Formulation services. Our platform provides access to organizations equipped with the expertise and technology necessary for the efficient and compliant production of finished pharmaceutical products.
Tablets
Tablets remain a cornerstone of oral drug delivery, known for their stability and ease of administration. Manufacturing tablets involves granulation, compression, and coating techniques, ensuring consistent drug release and patient compliance. They cater to a wide range of therapeutic needs, from pain management to chronic diseases.
Pharmaoffer lists Contract Development and Manufacturing Organizations (CDMOs) that excel in the production of tablets. As a mainstay in oral drug delivery, tablets are favored for their stability, ease of administration, and versatility in catering to various therapeutic needs. This includes specialized services in Tablets Manufacturing, tablet production, and GMP tablet manufacturing.
Key Services Provided by Our Listed CDMOs:
Granulation and Compression: Expertise in granulation processes to prepare powder for compression, and precision in tablet compression to ensure uniformity and dosage accuracy. This is a critical aspect of solid dose manufacturing.
Advanced Coating Techniques: Application of various coating techniques to enhance tablet stability, modify drug release, and improve patient acceptability. This is essential in tablet formulation.
Consistent Drug Release Profiles: Development of tablets with controlled release profiles, ensuring consistent therapeutic effects and patient compliance.
Custom Tablet Formulations: Capability to create customized tablet formulations, addressing a wide range of therapeutic areas from pain management to chronic disease treatment. This is a key service offered by tablet manufacturing companies.
Quality Assurance and Regulatory Compliance: Strict adherence to quality standards and regulatory guidelines, ensuring the safety and efficacy of tablet products. This includes adherence to GMP standards in tablet CDMO services.
Your Go-To Source for Tablet Production
Pharmaoffer connects you with CDMOs renowned for their tablet manufacturing capabilities. Whether for generic or specialized medications, our platform ensures access to providers equipped with the latest technology and expertise for high-quality tablet production.
Capsules
Capsules offer a versatile solution for oral drug delivery, particularly for drugs with taste or stability issues. Their production combines gelatin or vegetarian shells with active pharmaceutical ingredients (APIs), providing targeted release profiles. Capsules are essential in both over-the-counter and prescription medicine.
Pharmaoffer's selection of Contract Development and Manufacturing Organizations (CDMOs) includes experts in the production of capsules, a key component of oral drug delivery systems. Capsules are particularly valuable for drugs requiring taste masking or specific stability conditions. This includes specialized services in Capsule Manufacturing, capsule filling, and pharma capsule manufacturing.
Key Services Provided by Our Listed CDMOs:
Custom Capsule Formulation: Development of tailored capsule formulations, combining gelatin or vegetarian shells with APIs for specific release characteristics. This is a critical aspect of capsules formulation.
Taste Masking and Stability: Expertise in creating capsule formulations that address taste or stability issues, enhancing patient compliance and drug efficacy.
Targeted Release Profiles: Advanced technologies for creating capsules with precise release profiles, including immediate, delayed, or sustained release. This is essential in capsule contract manufacturing.
Compliance with Regulatory Standards: Adherence to global pharmaceutical manufacturing standards, ensuring high-quality and safe capsule products. This is a key service offered by Capsule Suppliers.
Versatile Production Capabilities: Capacity to produce a wide range of capsule types, catering to both over-the-counter and prescription medication markets. This includes expertise in capsules CDMO services.
Find Your Capsule Production Partner
On Pharmaoffer, you can connect with CDMOs that specialize in the innovative and efficient production of capsule formulations. Whether you're focusing on generic or novel drug development, our listed CDMOs offer the expertise and technology needed for high-quality capsule manufacturing.
Topical formulation
Topical formulations, including ointments and creams, are pivotal in dermatological treatments. Their production focuses on achieving the right consistency, absorption rate, and drug concentration for effective skin application, addressing conditions from eczema to infections.
Pharmaoffer features Contract Development and Manufacturing Organizations (CDMOs) with expertise in creating topical formulations, including ointments, creams, and gels. These products play a crucial role in dermatological treatments, offering targeted relief and treatment for various skin conditions. This includes specialized services in Topical Formulation, Topical Drug Manufacturing, and Topical Medication Manufacturing.
Key Services Provided by Our Listed CDMOs:
Optimized Consistency and Absorption: Development of formulations with the appropriate consistency and absorption rate, ensuring effective application and skin penetration. This is a critical aspect of Topical Drug production.
Precise Drug Concentration: Careful formulation to achieve the right drug concentration for maximum therapeutic effect while minimizing potential side effects. This is essential in Topical Drug development.
Diverse Dermatological Applications: Capability to produce a range of topical formulations for treating conditions such as eczema, psoriasis, infections, and more. This versatility is key for a topical CDMO.
Quality Control and Stability Testing: Rigorous quality assurance processes and stability testing to ensure the safety, efficacy, and longevity of topical products. This is a fundamental service of Topical Drug CDMO.
Patient-Centric Formulations: Focus on patient comfort and ease of use, enhancing patient compliance and treatment outcomes.
Find Your Topical Formulation Development Partner
Through Pharmaoffer, you can connect with CDMOs specializing in the development and manufacturing of topical formulations. Our platform provides access to experts who can deliver high-quality, effective topical treatments for a wide array of dermatological needs.
Oral Liquids
Oral liquids like solutions, syrups, and suspensions are vital for patients with swallowing difficulties. Their manufacturing ensures homogeneity, palatability, and stability, offering precise dosing in pediatric and geriatric care. They span a range of therapeutic categories.
Pharmaoffer features Contract Development and Manufacturing Organizations (CDMOs) that excel in the production of oral liquids, such as solutions, syrups, and suspensions. These formulations are particularly important for patients who have difficulties swallowing pills, including pediatric and geriatric populations. This includes expertise in oral liquids manufacturing, liquid pharmaceutical manufacturing, and liquid contract manufacturing.
Key Services Provided by Our Listed CDMOs:
Homogeneous Formulations: Ensuring consistent homogeneity in oral liquid formulations for uniform dosing and efficacy. This is a key aspect of oral liquids CDMO services.
Enhanced Palatability: Development of oral liquids with improved taste and texture to enhance patient compliance, particularly crucial in pediatric care. This is essential in liquid pharmaceutical manufacturing.
Stability and Shelf-Life: Focusing on the stability of formulations to ensure the longevity and effectiveness of oral liquids over time.
Precise Dosing Solutions: Offering solutions that allow for precise and adjustable dosing, accommodating different patient needs and treatment regimens. This is a critical service in liquid contract manufacturing.
Wide Therapeutic Range: Production capabilities spanning a diverse range of therapeutic categories to address various health conditions with oral liquid formulations. This includes Oral Solids manufacturing capabilities.
Your Partner in Liquid Formulation Excellence
Through Pharmaoffer, you have access to CDMOs with specialized expertise in the development and manufacturing of oral liquids. Our platform connects you with partners who can provide high-quality, patient-friendly formulations for effective and convenient treatments.
Suppositories
Suppositories offer an alternative route of administration, essential for patients unable to take oral medications. Produced using moldable bases that dissolve or melt at body temperature, they are used for pain relief, anti-nausea, and laxatives, ensuring patient comfort and efficacy.
Pharmaoffer connects you with Contract Development and Manufacturing Organizations (CDMOs) skilled in the production of suppositories. Suppositories provide a critical administration route for patients who are unable to take oral medications, offering an effective solution for various therapeutic needs. This includes specialized services in Suppository Manufacturing, Suppository Production, and Suppository CDMO.
Key Services Provided by Our Listed CDMOs:
Moldable Base Formulation: Expertise in creating suppositories using moldable bases that properly dissolve or melt at body temperature for efficient medication delivery. This is a key aspect of Suppository Manufacturing.
Diverse Therapeutic Applications: Production capabilities for a wide range of suppository applications, including pain relief, anti-nausea treatments, and laxatives. This versatility is essential in Suppository Production.
Patient Comfort and Efficacy: Focus on formulations that enhance patient comfort and ensure the efficacy of the active pharmaceutical ingredients.
Quality Control and Compliance: Adherence to pharmaceutical manufacturing standards, ensuring the safety and effectiveness of suppository products. This is a critical service of a Suppository CDMO.
Customized Development Solutions: Tailored suppository development to meet specific formulation requirements and patient needs.
Your Trusted Partner in Suppository Development
Through Pharmaoffer, pharmaceutical professionals can find CDMOs that specialize in the development and manufacturing of suppositories. Our platform ensures you have access to partners who can deliver high-quality, patient-friendly suppository products across various therapeutic categories.