LGM Pharma

We produce over 35 million doses of suppository forms yearly. Our GMP-compliant facility ensures each product is gentle, effective, and meets the highest quality standards.

Leading Suppositories Dosage Forms Manufacturing | LGM Pharma We are one of the leading suppository dosage forms manufacturers with a specialization in suppository formulation, development, and manufacturing. Contact LGM Pharma.

The Common Technical Document ( ), which compiles all relevant drug information into five modules, is critical to the approval of drugs. For a module to pass a review, it must adhere to strict international regulatory requirements.

Navigating Regulatory Landscapes: Simplifying Compliance To Streamline The Drug Approval Process - LGM Pharma The global regulatory landscapes for pharmaceutical and biopharmaceutical products are as complex as the therapies they govern. For manufacturers and sponsors

As the focuses on innovative quality management, pharmaceutical companies must adapt to evolving challenges in data integrity and supply chain efficiency.

Top Pharmaceutical Manufacturing Quality Challenges - LGM Pharma To pharmaceutical manufacturers, it may seem that quality has always been a key pillar of pharmaceutical development and manufacturing. Sometimes it is spoken

As the pharma industry advances with innovative drugs like biologics, new dissolution approaches are essential. What does the future hold for dissolution testing? Gain insights from Shailesh Vengurlekar, SVP of Quality and Regulatory Affairs at LGM Pharma, in his latest interview with Pharmaceutical Technology. https://www.pharmtech.com/view/dissecting-dissolution-testing

Dissecting Dissolution Testing Advances in dissolution testing equipment are helping to meet user demands to a certain degree; however, more innovation in the space may be necessary for novel therapies, such as biologics.

ODTs, or oral disintegrating tablets, are game changers for patients who have trouble swallowing. Finding the balance between dissolvability and durability is key to delivering safe, effective treatments.

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Drugs targeting serious illnesses are approved more quickly because of priority review routes, which drastically reduce conventional review times. These are essential for treatments that address pressing public health issues.

Navigating Regulatory Landscapes: Simplifying Compliance To Streamline The Drug Approval Process - LGM Pharma The global regulatory landscapes for pharmaceutical and biopharmaceutical products are as complex as the therapies they govern. For manufacturers and sponsors

Regulatory compliance, particularly for APIs, is a necessity. Partner with professionals who are experts in managing submissions and CFR compliance so you can concentrate on innovation.

Pharma & API Regulatory Services | API Sourcing Logistics LGM Pharma provides API Regulatory Services & Pharma Regulatory Support for all regulatory requirements in Pharmaceutical Industry. Contact for API shipping!

The dissolution testing landscape is evolving with advanced equipment and techniques. From autosampling capabilities to media that mimic physiological conditions, the industry is making significant strides. Read about the latest breakthroughs and their impact on the pharma sector in the latest interview with our own Shailesh Vengurlekar. https://lgmpharma.com/resources/ &D

Pharmaceutical CDMO | LGM Pharma Resources - LGM Pharma Find resources (white papers, case studies, articles) from LGM Pharma, a provider of active pharmaceutical ingredient (API) sourcing and CDMO services.

There are strict requirements for oral solid dose (OSD) formulations. The route from the laboratory to the pharmacy shelf can be determined by taking early measures to address stability, solubility, and patient compliance.

It’s A Simple Formula: Robust OSD Formulation = Successful Drug Product Fulfillment - LGM Pharma Oral solid dose (OSD) drugs are pharmaceutical preparations for oral administration in tablets, capsules, powders, or granules. They are mainly prescribed due

The timeframes for therapeutic approvals vary greatly globally. Effectively navigating each region's regulatory environment is necessary for strategic planning and a seamless introduction of new drugs into the market.

Navigating Regulatory Landscapes: Simplifying Compliance To Streamline The Drug Approval Process - LGM Pharma The global regulatory landscapes for pharmaceutical and biopharmaceutical products are as complex as the therapies they govern. For manufacturers and sponsors

Small molecule manufacturing is being redefined by niche drug development. If you’re looking for a CDMO, focus your search on three main areas: strong regulatory readiness, efficient raw material sourcing, and specialized production skills.

Outsourcing Analytical Testing: Three Problems To Avoid - LGM Pharma The need for greater capacity is indeed a common reason for seeking the support of a contract analytical laboratory. Many drug development companies keep

Dissolution testing plays a pivotal role in quality control and drug development. It assesses the absorption of a drug, ensuring consistent and reliable results. Explore the insights shared by Shailesh Vengurlekar from LGM Pharma on the importance of dissolution testing. Learn more here https://lgmpharma.com/resources/

Pharmaceutical CDMO | LGM Pharma Resources - LGM Pharma Find resources (white papers, case studies, articles) from LGM Pharma, a provider of active pharmaceutical ingredient (API) sourcing and CDMO services.

When it comes to API sourcing, quality assurance is more than simply a procedure — reputations are at stake. The highest standards are guaranteed for each batch through meticulous testing and quality inspections.

Navigating API Sourcing As A Pharmaceutical Manufacturer - LGM Pharma What will your sourcing team do when a challenge occurs with an active pharmaceutical ingredient (API)?

In addition to sourcing, we provide thorough support for guiding you through the challenges of drug manufacturing with market intelligence, regulatory advice, and logistical support.

Find Best API Sourcing Strategies & Solutions | LGM Pharma We are all here to help you to optimize your API Sourcing Strategies and our experts will provide you with a solution that is best for going on in the strategic api sourcing process.

The bottom line is any mishap in API sourcing can spell disaster for a contract development manufacturing organization.

Navigating API Sourcing As A Pharmaceutical Manufacturer - LGM Pharma What will your sourcing team do when a challenge occurs with an active pharmaceutical ingredient (API)?

Quality and safety drive everything we do at LGM Pharma. By integrating Quality by Design principles and maintaining rigorous validation processes, we ensure our pharmaceutical products are both effective and safe.

Catching up with LGM Pharma ahead of CPhI North America to find out about its pipeline LGM Pharma is a leading CDMO provider of comprehensive API sourcing and drug product contract development and manufacturing solutions to the pharmaceutical, biotechnology, and compounding pharmacy industries.

Gaining access to a large network of trustworthy manufacturers with frequent supplier inspections and strong quality control systems are some of the advantages to working with a skilled API sourcing partner for a drug development project.

Navigating API Sourcing As A Pharmaceutical Manufacturer - LGM Pharma What will your sourcing team do when a challenge occurs with an active pharmaceutical ingredient (API)?

We blend expertise, advanced technology, and comprehensive services to produce top-quality semi-solid pharmaceuticals from our state-of-the-art 54,000-square-foot facility in Rosenberg, Texas.

Semi-solid Dosage Pharmaceutical Forms Manufacturers | LGM Pharma LGM also offers all types of Semi-Solid Dosage Form manufacturing. Also, unit and bulk pharmaceutical packaging solutions for you!. Contact us now!

An effective combination of strategy and foresight is needed to navigate the challenges of sourcing. By managing risks, a trustworthy sourcing partner helps you keep your drug development projects on schedule.

Navigating API Sourcing As A Pharmaceutical Manufacturer - LGM Pharma What will your sourcing team do when a challenge occurs with an active pharmaceutical ingredient (API)?

We prioritize customer insights to stay ahead in the pharmaceutical industry. Our strategic investments in analytical testing and manufacturing capabilities ensure we meet the evolving needs of our clients.

Catching up with LGM Pharma ahead of CPhI North America to find out about its pipeline LGM Pharma is a leading CDMO provider of comprehensive API sourcing and drug product contract development and manufacturing solutions to the pharmaceutical, biotechnology, and compounding pharmacy industries.

If you are seeking insights into selecting the right CDMO for your next drug project, you’ll want to explore the advantages of boutique CDMOs over larger counterparts.

The Advantages Of A Boutique CDMO Vs. Challenges Of A Large CDMO: How To Choose The Right Partner - LGM Pharma Every decision counts in the world of drug development and manufacturing. When it’s time to entrust your drug development project to a contract development

From tablets and capsules to liquids and suppositories, LGM Pharma offers a comprehensive range of formulation and development capabilities to meet your molecule’s needs.

Pharmaceutical Formulation Development Services | LGM Pharma LGM pharma offers formulation development services from early development to clinical supplies, we mastered product development for FDA approval.

Project scalability and capacity are top concerns for drug sponsors evaluating CDMOs. Learning about the challenges and benefits of large and small CDMOs might help you with your decision making.

The Advantages Of A Boutique CDMO Vs. Challenges Of A Large CDMO: How To Choose The Right Partner - LGM Pharma Every decision counts in the world of drug development and manufacturing. When it’s time to entrust your drug development project to a contract development

Navigating the pharmaceutical supply chain can be as tricky as DIY renovations. Avoid the pitfalls of managing it yourself and consider outsourcing to API procurement specialists. https://lgmpharma.com/resources/white-papers/five-reasons-to-outsource-api-procurement/

Five Reasons To Outsource API Procurement - LGM Pharma Pharmaceutical development and manufacturing is an expensive business. Owners and managers, particularly those in young, lean firms with paper-thin margins,

Large vs. small CDMOs: What factors should you consider when selecting the right partner for your pharmaceutical project? Our latest blog post breaks it down.

The Advantages Of A Boutique CDMO Vs. Challenges Of A Large CDMO: How To Choose The Right Partner - LGM Pharma Every decision counts in the world of drug development and manufacturing. When it’s time to entrust your drug development project to a contract development

What are 5 reasons you should outsource API procurement? If you don’t want to DIY sourcing APIs, there is an alternative. You can partner with an API procurement and supply chain specialist. Download this white paper: https://lgmpharma.com/resources/white-papers/five-reasons-to-outsource-api-procurement/

Five Reasons To Outsource API Procurement - LGM Pharma Pharmaceutical development and manufacturing is an expensive business. Owners and managers, particularly those in young, lean firms with paper-thin margins,

Scalability, agility, and cost-effectiveness are factors to consider in choosing the right CDMO partner for your drug development journey.

The Advantages Of A Boutique CDMO Vs. Challenges Of A Large CDMO: How To Choose The Right Partner - LGM Pharma Every decision counts in the world of drug development and manufacturing. When it’s time to entrust your drug development project to a contract development

Orally disintegrating tablets (ODTs) offer increased patient compliance, portability, and bioavailability. But manufacturing ODTs comes with its own set of challenges.

The Advantages And Challenges Of Orally Disintegrating Tablets (ODTs) - LGM Pharma Taking medication can be a hard pill to swallow—but it doesn’t have to be! Orally disintegrating tablets (ODTs) have become increasingly popular due to their

Visit us at North America this week! Taking place from May 7-9 at the Pennsylvania Convention Center, Philadelphia. Join us at booth number 321 and let’s explore new collaboration opportunities. https://lgmpharma.com/about-lgm/events/

In drug development, size matters — but so does agility. Boutique CDMOs offer personalized attention and faster decision-making.

The Advantages Of A Boutique CDMO Vs. Challenges Of A Large CDMO: How To Choose The Right Partner - LGM Pharma Every decision counts in the world of drug development and manufacturing. When it’s time to entrust your drug development project to a contract development