Pharmaceutical and Biotech Regulatory Solutions
  • How can you get your product to market as quickly and efficiently as possible?

    It's with a sound Regulatory Strategy

    We can put you on the right path

    Get Started
  • We are dedicated to the

    Discovery, development &
    commercialization

    Of innovative products bringing broad therapeutic knowledge, an in-depth understanding of global/local market landscapes and regulatory guidelines to generate customized strategies to meet your needs from early-stage development to lifecycle management

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  • Looking for an opportunity where scientific progress could accelerate the development and approval of generic products?

    Put your confidence in collaborative and quality by design solutions

    You can count on us to get your product to market

    Discover How

Welcome to Aim BioPharma

Aim BioPharma works with you to develop an effective strategy to optimize time to market of your products. We are especially dedicated to support you with new ideas and in bringing forward innovative therapies.

Our team will use our years of experience to provide you with expert strategic guidance in Pharmaceutical Development, Manufacturing, Quality, Clinical & Non-Clinical, Stability & Storage, Validation, Packaging & Labeling, Pharmaceutical excipients, Impurities, Safety & Pharmacovigilance (PV), Warnings and Submission Formats.  We can help you navigate through the demanding complexity of the diverse Regulatory requirements.

Project Management

Management of various discovery, development, testing and manufacturing processes within a highly-regulated and controlled environment. Our goal is success with all the projects we manage.

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GMP Audits

Performing a Good Manufacturing Practice (GMP) audit of the facility and review of processes, procedures, systems, and facilities to enhancing the level quality and building on the systems that are already in place.

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Quality Systems & Management

Optimizing the quality management system and identifying gaps to align operating procedures, root cause analysis, cross-functional CAPA management, and training.

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Regulatory Strategy

Our team provides a roadmap to getting your product to market with Health Canada, FDA and EMA consent, handling regulatory submissions, renewals, notifications and amendments.

Next Step

Development Pipeline

Balancing a mix of experience and life cycle management.

We focus on core competencies and project management. We bring discovery, development, testing and manufacturing processes to the table.

01

Discovery

02

Starting Phase

03

Mid Phase

04

Final Phase

05

Product Approval

06

Product Production

Why Aim BioPharma?

About Us
Experience and Resources

We manage the discovery, development, testing and manufacturing of your product.

Good Manufacturing Practice

We perform GMP audits to ensure compliance and quality.

Accuracy and Quality

We optimize the functionality of systems to improve speed and quality.

Amazing Customer Service

Prompt returned calls and emails. Customers are #1 at Aim Biopharma!

Industries We Serve

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