Custom Pharma Services (CPS) as a strategic business unit of Dr Reddy’s draws on years of knowledge and expertise in pharmaceutical development and manufacturing to provide innovators with customised services and solutions for intermediates, active ingredients and finished dosages. Within a short span, we have become one of the largest pharmaceutical outsourcing players from India and a global partner-of-choice. We have a track record of bringing innovations to the market quickly, efficiently and economically with the capability to supply both small-scale clinical trial quantities and commercial-scale requirements. Our end-to-end services make a compelling value proposition to our global innovator customers.
No data available
EIP is an innovative Intellectual Property law firm advising on all areas of IP. EIP has more than 60 professional staff practising from its four UK offices in Bath, Cardiff, Leeds and London, its US office in Denver and its German office in Dusseldorf. EIP Life is our life sciences and medical devices team which has a wealth of technical knowledge and experience in dealing with the biotechnology and health sectors, for start-ups and major multinationals.
Lilly is developing a growing portfolio of best in class pharmaceutical products by applying the latest research from our own laboratories and from collaborations with eminent scientific organisations worldwide. In 2003 the company's world-wide sales were more than $12 billion. Lilly employs more than 43000 people worlwide and markets medicines in 158 countries. Lilly Research Laboratories (the R&D division of the company) employs more than 8000 people from a wide variety of disciplines. The company has R&D facilities in 9 countries and currently conducts clinical trials in more then 60 countries around the world. . . Lilly's internal research efforts are focused in the following major therapeutic areas: cancer, cardiovascular diseases, endocrinology, neuroscience, gene regulation, bone biology, immunomodulation and Inflammation Compounds in late stage development, and those currently being launched have promise to address the needs of patients with sepsis, cancer, diabetes, depression, osteoporosis, erectile dysfunction, urinary incontinence and attention deficit hyperactivity disorder.. . In pursuit of innovation Lilly seeks to incorporate those cutting edge technologies which support the high quality, rapid identification and investigation of novel compounds.. . The company approach to innovation includes a commitment to the philosophy of research without walls - a stated commitment to partnership and external collaboration. Currently Lilly Research Laboratories has more than 120 active collaborations with external scientists.
Watch our Member Showcase video here https://bit.ly/3HZGpJI
The mission of EMBL-EBI is to: provide freely available data and bioinformatics services to all facets of the scientific community in ways that promote scientific progress; contribute to the advancement of biology through basic investigator-driven research in bioinformatics; provide advanced bioinformatics training to scientists at all levels; and help disseminate cutting-edge technologies to industry. . The research and service activities of EMBL-EBI span the entire spectrum of life science and remain at the cutting edge of the computational sciences. All our major data resources are the products of international collaborations. We work with other data providers to ensure that our data repositories, and those of our collaborators, are comprehensive and up to date. We also actively participate in international efforts to develop data standards.. . The EMBL-EBI Industry Programme engages our industrial users with the latest bioinformatics research, service development, standards activities, pre-competitive opportunities and training https://www.ebi.ac.uk/industry.
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Strategic and finance advisory
Immunotherapeutics company targeting a new class of tumour specific antigens
Eramol | UK Sterile Fill-Finish and Non-Sterile Pharmaceutical Manufacturing CMO
Eramol is an independent UK and EU pharmaceutical contract manufacturing organisation supporting biotechnology, pharmaceutical, academic and investigator-led clinical programmes. Founded, owned and led by Qualified Persons, Eramol provides integrated pharmaceutical manufacturing and clinical-supply services across sterile and non-sterile drug products. Sponsors can access GMP manufacturing, clinical packaging, labelling, QC testing, QP certification, storage and global distribution through one accountable partner.
Sterile fill-finish and injectable manufacturing
Eramol’s purpose-built Sevenoaks facility provides early-phase sterile fill-finish services for injectable drug products, with a focus on Phase I and Phase II clinical-trial supply.
The facility has been designed around EU GMP Annex 1 principles and includes Grade A isolator technology, closed single-use processing, sterile filtration, aseptic processing and moist-heat terminal sterilisation.
Eramol’s aseptic fill-finish capability with <0.1% line losses is engineered to protect scarce and high-value drug substance. This is particularly valuable for early-phase biologics, monoclonal antibodies, antibody-drug conjugates, peptides, oligonucleotides, RNA therapeutics, viral vectors and other complex injectable products where conventional filling losses can materially affect programme cost and available clinical supply.
The flexible small-batch model supports sterile vials, cartridges and pre-filled syringes, with manufacturing designed for programmes requiring technical agility, high filling accuracy and maximum product recovery.
Non-sterile pharmaceutical manufacturing
Eramol’s established Sevenoaks non-sterile pharmaceutical manufacturing facility supports clinical development through to commercial supply.
GMP manufacturing capabilities include:
• Active and placebo tablets
• Coated and uncoated tablets
• Hard-shell capsules
• API neat-fill capsules
• Over-encapsulation and comparator blinding
• Oral solutions and suspensions
• Placebo development and sensory matching
• Clinical and commercial batch manufacture
The facility supports Phase I, Phase II and Phase III programmes, together with commercial manufacturing requirements. Integrated placebo manufacture and blinding capabilities help sponsors maintain study integrity across complex randomised clinical trials.
Integrated clinical manufacturing and supply
Eramol combines sterile and non-sterile manufacturing with clinical packaging services, multilingual labelling, analytical testing, stability support and regulatory oversight.
In-house Qualified Persons provide UK and EU QP release and certification for clinical and commercial products. Through its UK facilities and Dublin EU hub, Eramol can support manufacture, importation, certify and release for supply across the United Kingdom and European Union.
Following QP release, Eramol provides clinical storage and global pharmaceutical distribution, including controlled ambient, refrigerated and frozen storage, validated cold-chain distribution, direct-to-site supply and international clinical logistics.
This integrated model gives sponsors one experienced partner from pharmaceutical manufacturing through to QP release and delivery to clinical sites.
Watch the video here: https://shorturl.at/8VmLC
For more information see: https://eramol.com/ & https://eramol.com/clinical-services-category/sterile-fill-finish/
Eramol is an independent UK and EU pharmaceutical contract manufacturing organisation supporting biotechnology, pharmaceutical, academic and investigator-led clinical programmes. Founded, owned and led by Qualified Persons, Eramol provides integrated pharmaceutical manufacturing and clinical-supply services across sterile and non-sterile drug products. Sponsors can access GMP manufacturing, clinical packaging, labelling, QC testing, QP certification, storage and global distribution through one accountable partner.
Sterile fill-finish and injectable manufacturing
Eramol’s purpose-built Sevenoaks facility provides early-phase sterile fill-finish services for injectable drug products, with a focus on Phase I and Phase II clinical-trial supply.
The facility has been designed around EU GMP Annex 1 principles and includes Grade A isolator technology, closed single-use processing, sterile filtration, aseptic processing and moist-heat terminal sterilisation.
Eramol’s aseptic fill-finish capability with <0.1% line losses is engineered to protect scarce and high-value drug substance. This is particularly valuable for early-phase biologics, monoclonal antibodies, antibody-drug conjugates, peptides, oligonucleotides, RNA therapeutics, viral vectors and other complex injectable products where conventional filling losses can materially affect programme cost and available clinical supply.
The flexible small-batch model supports sterile vials, cartridges and pre-filled syringes, with manufacturing designed for programmes requiring technical agility, high filling accuracy and maximum product recovery.
Non-sterile pharmaceutical manufacturing
Eramol’s established Sevenoaks non-sterile pharmaceutical manufacturing facility supports clinical development through to commercial supply.
GMP manufacturing capabilities include:
• Active and placebo tablets
• Coated and uncoated tablets
• Hard-shell capsules
• API neat-fill capsules
• Over-encapsulation and comparator blinding
• Oral solutions and suspensions
• Placebo development and sensory matching
• Clinical and commercial batch manufacture
The facility supports Phase I, Phase II and Phase III programmes, together with commercial manufacturing requirements. Integrated placebo manufacture and blinding capabilities help sponsors maintain study integrity across complex randomised clinical trials.
Integrated clinical manufacturing and supply
Eramol combines sterile and non-sterile manufacturing with clinical packaging services, multilingual labelling, analytical testing, stability support and regulatory oversight.
In-house Qualified Persons provide UK and EU QP release and certification for clinical and commercial products. Through its UK facilities and Dublin EU hub, Eramol can support manufacture, importation, certify and release for supply across the United Kingdom and European Union.
Following QP release, Eramol provides clinical storage and global pharmaceutical distribution, including controlled ambient, refrigerated and frozen storage, validated cold-chain distribution, direct-to-site supply and international clinical logistics.
This integrated model gives sponsors one experienced partner from pharmaceutical manufacturing through to QP release and delivery to clinical sites.
Watch the video here: https://shorturl.at/8VmLC
For more information see: https://eramol.com/ & https://eramol.com/clinical-services-category/sterile-fill-finish/