A Reliable Partner in Pharmaceutical Manufacturing and Development
Experienced Specialists at Your Side
Our most valued asset is our proficient specialists, whose combined expertise encompasses all aspects of pharmaceutical development and operations. The experience profile of our scientists ranges from 15 to 35 years, with over 250 ANDA approvals and hundreds of successful formulations of NCEs developed and cGMP clinical trial materials manufactured.
Our regulatory and compliance support services include, but are not limited to, the filing of INDs, NDAs, ANDAs, resolution of FDA deficiencies, and site pre-approval inspection readiness. We serve a diverse group of clients globally as regulatory agents to assist with the registration of their facilities and their products with the US FDA and foreign health ministries. Our Technical Service Group provides on-site services to resolve manufacturing process issues and provide consultation for the qualification of equipment and laboratory instruments.
Our facility, registered with the Food and Drug Administration (FDA), is operated under current Good Manufacturing Practices (cGMPs) and an independent Quality Assurance program.
Our Facilities
Miami, Florida
Allay Pharmaceuticals, LLC. conducts operations from its facility located in an industrially zoned business park in Miami, Florida. This facility functions as the corporate headquarters as well as the central hub for all technical operations. After recent expansions, the facility now consists of several independent units, with a total operating space of more than 16,000 square feet.
The manufacturing wing features six process rooms, each designed for specific process requirements with full isolation and containment. These suites are capable of supporting volumes anywhere between small-scale product development and commercial-scale manufacturing.
The analytical wing consists of three analytical laboratory suites, all equipped with state-of-the-art analytical instrumentation to support our clients' needs.
The facility features two spacious warehouse areas with incoming and outgoing material-handling processes and a secure controlled-substance holding area in compliance with DEA requirements. Elaborate operating procedures are enforced to run the facility in accordance with GMP guidelines.
Dhaka, Bangladesh
Allay has expanded its business internationally and has established a branch office in Bangladesh to develop long-term customer relations with its existing clients. The office is located in the capital city of Dhaka.
Mississauga, ON, Canada
This is one of our newer offices. More information will be coming soon.
Our Licenses and Compliance
About Our Pharmaceutical Manufacturing Team
Allay Pharmaceuticals LLC has been serving the industry since 2006. The company was founded by a group of highly competent professionals who are former employees of many of the top pharmaceutical companies in the United States. The experience profile of the multi-faceted management team includes:
Technical
- Analytical Development and Lab Testing
- Formulations and product development
- Manufacturing Processes
- Packaging
- Engineering
- Information Technology
- Administrative
Quality Control
- Quality Assurance
- Regulatory Affairs and Compliance
- NDA and ANDA submissions
- FDA, DEA, EPA, and OSHA regulations
- Entrepreneurial experience
- Business and financial operations
Our Vision
Through our diverse professional skills, clarity of purpose, and values, we aim to set a dynamic attitude to steer Allay to lead market trends in pharmaceutical services and to achieve sustainable growth for our company through client relations.
Establishing and monitoring customer requirements is the foundation for Allay's Quality Program and provides objective measures of Allay's performance. We will continue to work with and listen to our customers, with a focus on ensuring that their satisfaction remains a top corporate priority. Allay executives are responsible for creating and sustaining a clear and visible quality program, along with a supporting management system, to guide all activities of the company. We are dedicated to maintaining an environment that is conducive to full employee participation, continuous improvement, and personal and organizational growth.
Allay envisions establishing itself as a market leader in the pharmaceutical service business. One of Allay's top priorities is creating and preserving customer satisfaction. Customers are involved at every stage of the process in order to determine their needs and the key features to be integrated into our services.
We respect the needs and expectations of our internal and external customers, and we are committed to providing the product our customers demand with the service they expect from the people they can depend on.
Precision and trust define the technical consulting services we provide to clients across Fort Lauderdale. By choosing us, you tap into a team with extensive expertise ensuring every project meets the highest standards through tailored technical consulting services designed to solve complex engineering challenges. Our technical consulting services guarantee reliable results that support operational efficiency and product safety, instilling confidence throughout your development process. In Fort Lauderdale, FL, organizations rely on our cutting-edge technology and experienced staff to deliver technical consulting services that drive informed decisions. Partner with us for technical consulting services that elevate your projects and demonstrate uncompromising quality at every step.
Offering Career Opportunities
We believe that the training and development of team members in a culture of strict quality and compliance is critical to upholding Allay's brand image and serving the industry in general. Allay is constantly scouting for bright and talented individuals to join our team. Please contact us to inquire about available positions.
OUR OTHER SERVICES
Formulation Development
Solids (IR/ER/DR/Sublingual, Buccal)
Semi-solids (topical and transdermal)
Liquids (Solutions and Suspensions)
Transdermal (Patches)
Drug Delivery
Custom technology development
Platform or Individual Molecule-Based
Sole Proprietary or Out-Licensed
All Major Dosage Forms
Risk-sharing arrangements
Poorly Soluble Compound Expertise
Immediate/Delayed/Extended Release
Sublingual and buccal delivery platforms
Contract Manufacturing
(GMP and GLP)
Commercial volume manufacturing of solid-dose products
Single- and tri-layer tablet compression capabilities
Batches to support Proof of Concept Studies
CTM Manufacturing for Phase I and Phase II NCEs
Pilot and pivotal batch manufacturing of ANDAs (~100 kg scale)
Manual Packaging and Labeling of CTMs
Global Regulatory Services
IND, NDA, and ANDA submissions
Foreign Facility and Product Registration
US Regulatory Agent Representation
Post-approval change consultation
FDA meeting plans and meeting participation
Compliance Services
FDA 483, warning letters
Consent decree resolution
Assistance with site inspection readiness (including pre-approval inspections)
Training (the curriculum is custom-developed per the client's choice)
Quality System Audits
Analytical Testing
Complex Method Development
Method Validations and Transfers
Testing of Raw Materials and Finished Products
Stability, Storage, and Testing
