We are one of the fastest growing organization in corporate health, Digital health solution and at home healing
Cellula's Regulatory Affairs group is a specialty logical and administrative counseling bunch. We guide and help drug, biotech and medical organizations in the plan and execution of creative and worldwide administrative procedures to assist item improvement and enrollment of medications, biologics, clinical gadgets, mix items, and other medical services items for all progressive phases
Cellula has broad involvement with getting ready post-market reconnaissance (PMS) reports. Our PMS specialists comply with rules like the European Medicines Agency (EMA), Food and Drug Administration (FDA), and other neighborhood country rules
With an expanded spotlight on research plan and admittance to best in class information assortment advancements, the medication disclosure industry is building an establishment on proof based, information driven experiences. Cellula's group of biostatistics and measurable software engineers gives you the functional and key insights required for each part of medication improvement
Investigator Initiated Studies
We assist our clients with planning and execute review and imminent examinations to distribute clinical results, make specialized papers on treatment methods, and introduce and distribute case audits. Clinical Trial Data can give the proof to drive clinical choices for ideal patient consideration.
Clinical Writing is an essential piece of clinical examination and our group of expert clinical scholars convey exact, opportune, and savvy clinical and administrative reports to the best and logical norms.