Clinical trials for patients at the highest level of quality

Our approach is uncompromising – each study conducted at our site is carefully planned and executed according to protocol and regulations with superior quality.

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Our Clinic

IN-VIVO is a multi-specialty Clinical Research Center founded in 2017 in Bydgoszcz, Poland. Conducting Phase II through Phase IV studies in a large variety of medical specialties.

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Experienced and adequately trained medical staff includes Investigators, Study Nurses, Study Coordinators and a Research Site Manager.
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Paper and electronic type of source documentation. The electronic system is compliant with the following regulations: FDA 21, CFR Part11, EMA, GCP ICH and GDPR

We have experience conducting clinical trials

in many therapeutic areas, particularly..

Cardiology

Cardiac arrhythmias

Hypertension

Prevention of cardiovascular events in high-risk patients

Cardiac failure

Diabetology

Type 1 and type 2 diabetes

Diabetic retinopathy

Diabetic nephropathy

Overweight & obesity

Gynecology

Endometriosis

Uterine myoma

Vasomotor symptoms associated with menopause

Gynecological oncology

Fertility disorders

Hematology

Hodgkin's Lymphoma

Non-Hodgkin's Lymphomas (SLL, MZL, FL, MCL, DLBCL)

Chronic Lymphocytic Leukemia

Chronic Myeloid Leukemia

Acute Myeloid Leukemia

Paroxysmal Nocturnal Hemoglobinuria

Immune Thrombocytopenia

Myelofibrosis

Essential Thrombocythemia

Polycythemia vera

Multiple Myeloma

Infectious disease

(prevention and treatment of children, adolescents and adults), caused by e.g.:

Meningococci

Pneumococci

COVID-19

Influenza

Varicella

Respiratory Syncytial Virus (RSV)

Oncology

Genitourinary cancers (kidney, bladder, prostate, ovarian, endometrium)

Orthopedics

Degeneration of the spine

Pain syndrome

Pediatrics & Neonatology

Allergies (e.g. hypoallergenic modified milks)

Skin diseases

Gastrointestinal diseases (GERD, treatment prevents regurgitation)

Anemia

Psychiatry

Depression

Post Traumatic Stress Disorder (PTSD)

Bipolar disorder

Schizophrenia

Urology

Erection disorders

Micturition disorder, including urinary incontinence

The personnel responsible for the collection, preparation and shipment of biological material regularly participate in IATA training

All members of the team are required to follow ICH GCP requirements, EU, Polish legislation and Company’s Standard Operating Procedures (SOPs)

Anna Nodewald

Administrative manager

Contact

Organizational matters

Independent Ethics Committee (IEC)

N-VIVO belongs to IEC at the medical council in Bydgoszcz. The committee meets a regular intervals every 4 weeks. 

Contract

A quick, efficient process. The average duration of time, from starting negotiations to signing the contract is 28 days.

Inspections and Audits

Since 2020 IN-VIVO has underwent 7 audits. The Principal Investigators who cooperate with our Center have experience in FDA, Polish routine regulatory inspections and audits.