All Departmental Services – Gilead Life Sciences

Commercial Manufacturing

We offer comprehensive commercial pharmaceutical manufacturing services designed to meet the needs of pharmaceutical companies and healthcare providers worldwide. With state-of-the-art facilities and a team of experienced professionals, we specialize in producing high-quality medications at scale while ensuring strict compliance with global regulatory standards.

Our services begin with the seamless transition from research and development to full-scale production. We work closely with our clients to optimize formulations and manufacturing processes, ensuring cost efficiency without compromising on quality. Whether it’s solid dosage forms like tablets and capsules, liquid formulations, or specialty products, our advanced equipment and cutting-edge technology guarantee precision and consistency in every batch.

We prioritize quality at every stage of manufacturing. Our facilities are fully compliant with Good Manufacturing Practices (GMP), equipped with sterile environments and real-time monitoring systems to maintain the highest standards of safety and product integrity. Every product undergoes rigorous quality testing, ensuring it meets all required specifications before reaching the market.

Scalability is a cornerstone of our services. From small pilot batches to large-scale production runs, we have the expertise and capacity to meet the growing demands of our clients. Our efficient production lines are designed to handle high-volume output without delays, ensuring timely delivery to markets worldwide.

In addition to manufacturing, we provide comprehensive packaging and labeling services. Our solutions include tamper-evident packaging, serialization, and compliance with regional regulatory requirements, ensuring your products are market-ready and patient-friendly.

As part of our commitment to innovation, we integrate the latest advancements in automation, artificial intelligence, and machine learning into our manufacturing processes. These technologies enhance efficiency, reduce waste, and ensure that our clients benefit from the highest levels of quality control and operational excellence.

We also recognize the importance of sustainability in modern pharmaceutical manufacturing. Our processes are designed with eco-friendly practices, such as energy-efficient production lines and waste reduction systems, to help our clients meet their sustainability goals while delivering life-saving medications to patients.

With [Your Company Name] as your manufacturing partner, you can trust us to deliver reliable, scalable, and high-quality solutions tailored to your unique requirements. Together, we can bring innovative healthcare solutions to life and make a meaningful impact on global health.

Formulation Development

We provide comprehensive formulation development services designed to transform innovative concepts into safe, effective, and market-ready pharmaceutical products. Our expertise lies in developing robust formulations that meet therapeutic goals, regulatory requirements, and commercial objectives.

The formulation development process begins with an in-depth understanding of the active pharmaceutical ingredient (API) and its properties, such as solubility, stability, and bioavailability. Leveraging this knowledge, our team of scientists and formulation experts carefully selects excipients and designs formulations optimized for performance, patient compliance, and scalability.

We specialize in a wide range of dosage forms, including oral solids (tablets and capsules), liquids, injectables, topical formulations, and specialty drug delivery systems. Each formulation is designed with precision to ensure efficacy, stability, and ease of administration.

Our advanced facilities are equipped with state-of-the-art technology to support every stage of development, from pre-formulation studies to pilot-scale manufacturing. We conduct comprehensive compatibility and stability studies to ensure that each formulation meets the highest standards of safety and reliability.

Regulatory compliance is a cornerstone of our formulation development services. We work in alignment with global regulatory requirements, ensuring that all documentation, testing, and processes are ready for approval by agencies such as the FDA, EMA, and others. Our detailed reports and thorough validation processes minimize delays, allowing for faster time-to-market.

Innovation is at the heart of our approach to formulation development. Whether it’s developing novel drug delivery systems, enhancing bioavailability of poorly soluble APIs, or improving the stability of complex formulations, we utilize cutting-edge techniques and technologies to achieve optimal results.

As a trusted partner, we focus on tailoring solutions to the unique needs of each client. From optimizing existing formulations to creating entirely new ones, we deliver results that align with your therapeutic and business goals.

Choose us for your formulation development needs and benefit from our scientific expertise, advanced facilities, and unwavering commitment to quality and innovation. Together, we can bring your pharmaceutical vision to life and deliver impactful healthcare solutions to the world.

Bioanalysis

we offer world-class bioanalysis services to support pharmaceutical and biopharmaceutical development at every stage. Our comprehensive solutions are designed to deliver accurate, reliable, and timely data essential for evaluating the safety, efficacy, and pharmacokinetics of drugs and biologics.

Our bioanalysis services specialize in the quantitative and qualitative measurement of drugs, metabolites, and biomarkers in various biological matrices such as plasma, serum, urine, and tissues. Using advanced analytical technologies, we ensure high sensitivity, specificity, and reproducibility for even the most complex compounds.

With a focus on innovation and precision, our team employs cutting-edge techniques such as Liquid Chromatography-Mass Spectrometry (LC-MS/MS), Gas Chromatography-Mass Spectrometry (GC-MS), and immunoassay platforms. These methods enable us to support a wide range of studies, including pharmacokinetic (PK), pharmacodynamic (PD), bioequivalence (BE), and toxicokinetic (TK) assessments.

Regulatory compliance is a fundamental aspect of our bioanalysis services. Our laboratory operates under strict Good Laboratory Practices (GLP) and adheres to international regulatory guidelines set by agencies like the FDA, EMA, and ICH. We provide detailed and fully compliant documentation to streamline regulatory submissions, reducing time-to-approval for your drug development program.

Our experienced bioanalytical scientists work closely with clients to design tailored study protocols and provide end-to-end support. From method development and validation to sample analysis and data interpretation, we ensure that every step of the process meets the highest quality standards.

As your trusted partner,we combines scientific expertise, advanced technology, and a commitment to excellence to deliver bioanalysis services that accelerate your drug development journey. Whether you’re conducting preclinical studies or large-scale clinical trials, we provide the data and insights you need to make informed decisions and bring life-changing therapies to market.