The CDMO Division of Lubrizol Life Science Health (LLS Health) is a leading pharmaceutical contract development and drug product manufacturing organization. With a range of technical capabilities, multiple technology platforms, and expertise in complex drug delivery, we can take on your formulation and production challenges.
Our hands-on approach and passion for knowledge sharing helps to find the best solution to deliver your project successfully.
A CDMO for all phases
CDMO
COMMERCIAL
CLINICAL
FORMULATION
ANALYTICAL
Choose your section below to tour our virtual environments with further information and a deeper dive into our technology and labs.
Chromatography Lab
Physical
Characterization Lab
Sample Preparation Lab
Drug-Eluting Device Lab
Process Lab
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Quality Control Lab
Commercial Viewing
Corridor
Process Room
Lyophilization Room
Clean Room A
Stability Room
Clean Room B
Clean Room C
GMP Warehouse
Formulation Lab
The site of most sterile GMP manufacturing for clinical trial materials. This cleanroom features a cascading design that contains ISO 8, ISO 7, and ISO 5 space, including a laminar flow hood.
This area has been used to fill 2 to 200 mL vials, 5 and 10 mL ophthalmic bottles, and other aseptically manufactured and terminally sterilized products.
Cleanroom A - Clinical Manufacturing of Sterile Products
The site of most sterile GMP manufacturing for clinical trial materials. An ISO 5 space designed for commercial lyophilization, it includes a pass-through from our filling room.
Commercial Lyophilization Room
Clean Room D
An ISO 7 cleanroom designed for highly potent compound handling. The cleanroom serves as a large, flexible processing space to accommodate complex equipment trains and large pieces of equipment, such as hot melt extruders.
Cleanroom B - Highly Potent Compound Handling
A 1400 square foot cleanroom containing 5 separate manufacturing suites, including a clinical GMP lyophilizer. It is used for both sterile and non-sterile manufacturing (ISO 7 and ISO 5 areas).
The processing suite is equipped with SIP/CIP to enable aseptic processing. This area is also qualified for filling 1 mL and 3 mL pre-filled syringes.
Cleanroom C - Clinical Manufacturing of Sterile Products
An ISO 7 cleanroom designed for highly potent compound handling. Similar to Cleanroom B, this is a flexible processing space with a high ceiling capable of accomodating large manufacturing equipment.
Cleanroom D - Highly Potent Compound Handling
Filling Room
A large, ISO 7 processing area with ample utilities and clean-in-place/steam-in-place capability.
It is designed to be a modular, flexible space to accommodate a range of processing and formulation equipment.
Commercial Process Room
An ISO 5 space designed for aseptic fill and finish operations.
It enables commercial vial and bottle filling with no minimum batch sizes.
Commercial Filling Room
