Service Offerings

 Our company understands that technology and medicine in the health care industry is consistently progressing. Our team of experienced professionals  stay current about the latest drug trends. 

  Long term partnerships with production facilities (CMO's) across the world covering a range of product types and dosage forms, you can count on our manufacturing expertise to reliably deliver your product on time, every time. We maintain the highest level safety when it comes to testing, manufacturing and transferring of products. 

Having decades of hands-on development experience with a wide range of (complex) technologies and the complete scale of finished dosage forms, are able to fully execute and/or support the development of any finished dosage form, formula or process, as well as the transfer and scale-up of a developed product to a cGMP manufacturing facility. 

 Our team is constantly keeping up with medical trends and technology and strive to find better ways to improve the health of our patients in an ever-changing industry. 

We are committed to being the foremost partner and leading supplier of innovative dosage forms and solutions to the healthcare industry. Throughout each phase of the drug and device development and manufacturing lifecycles, companies are faced with significant compliance challenges.

Our quality assurance expertise includes industry regulation and compliance, risk identification and mitigation, processes, and training. This practice also yields corporate strategies, insightful analysis for performance improvement, quality training programs to support business needs, and audits to verify compliance.

  Whether you’re a large or small pharmaceutical company, our talented team can develop and transform your promising molecule into a product. 

We’ve supported many clients over the years, and you can be next. Our team is constantly keeping up with medical trends and technology and strive to find better ways to improve the health of our patients in an ever-changing industry. 

We continuously strive to exceed client expectation during projects with emphasis on quality and fast turnaround time. This is managed by a team of skilled and experienced personnel in Project Management who complete each project as per pre-defined timelines.

We work to earn your trust for a long lasting & fruitful business partnership with complete value for money and desired level of performance.

 We provide our clients with GLP and GMP services including auditing, inspection preparation, Inspection remediation and QA support 

We are proficient, focused and specialized in offering end-to-end support services to pharmaceutical companies having a vision to reach and to grow in regulated market.

Our Services has expertise in ensuring wide-ranging support with high quality and cost-effective solutions in critical areas of pharmaceutical business. Our talent pool is enriched with extensive knowledge and far-reaching industrial experience in handling complex issues from early phase of product development until regulatory approvals and post-approval life-cycle management.

Our services includes local agent representation, strategic regulatory submission planning, due-diligence, global regulatory submissions, clinical services and manufacturing facility audits. We carefully evaluate our customer’s need and customize our services.

  Our project management experience technologies and processes are advanced and robust. This means that your interests will be vigorously represented by high-performance teams who have a proven track record, the know-how and the project management systems to deliver your project in ways that minimises risk and to high quality standards. 

 BioInnova operates a pharmaceutical warehouse and storage facility in NSW, Australia backed up by a professionally run distribution network. Exports across five continents, is vindication of BioInnova’s commitment to quality, and global acceptance by discerning Hospitals , GP's and clients.