We get hospitals, because we were created by one.

IntegraDose was started to solve a simple hospital need: to get the most commonly compounded medications to patients as quickly, accurately and efficiently as possible. We deliver compounded products more efficiently, so you can care for your patients more effectively.

Why IntegraDose?

From Hospitals for Hospitals

We are a health system-owned facility. Everything we make and sell has been proven in our own hospitals.

Reliability Guaranteed

We maintain a large stock of raw materials and finished inventory to mitigate shortage and supply chain risks.

State-of-the-Art Facility

Our 503B compounding facility effectively meets or exceeds all regulations with five cleanrooms and both on-site and external lab testing to guarantee quality prior to release.

Dependable Inventory

Thanks to our health system infrastructure, we’re the ones who have access to products that others can’t or won’t supply.

Sterile to Sterile Products

All components of our products begin as sterile to eliminate potential contamination issues resulting in the safest products from start to finish.

No Quotas or Volumes

No commitments or obligations on quantities gives you hassle-free ordering for only what you need and no more.

Faster Fulfillment

We compound our medications in anticipation of need, based on our knowledge of patient volumes. That focus means we can get our products to you faster—usually in a day—than most other 503B compounding pharmacies.

One Price For All

What you pay is what we pay so you are always guaranteed clear and easy costs that fit your budget.

Our Products

We can treat your hospital’s pain points by changing how you provide care to your patients.

Our compounded products are designed to anticipate your needs, minimize drug shortages and are typically stable for months—instead of mere hours—and both on-site and external lab testing are used to ensure potency, endotoxin, and sterility prior to release.

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Phenylephrine Hydrochloride 1000 mcg/10 mL in 0.9% Sodium Chloride
NDC: 71139-7084-1
Syringe for Injection (Concentration 100 mcg/mL)
10 mL Syringe - 10 mL Fill
BUD: 180 Days Room Temp
Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride
NDC: 71139-0190-1
Syringe for Injection (Concentration 1 Unit/mL)
3 mL Syringe - 2 mL Fill
BUD: 180 Days Room Temp
Sugammadex 200mg/2mL
NDC: 71139-5355-1
Syringe for Injection (Concentration 100 mg/mL)
3 mL Syringe – 2 mL Fill
BUD: 60 Days Room Temp
Sugammadex 100mg/1mL
NDC: NDC: 71139-5355-2
Syringe for Injection (Concentration 100 mg/mL)
3 mL Syringe – 1 mL Fill
BUD: 60 Days Room Temp
Fentanyl Citrate 200 mcg/100 mL + 0.1% Ropivacaine in 0.9% Sodium Chloride
NDC: 71139-5340-4
CADD for Injection (For Epidural Use)
100 mL CADD Cassette - 100 mL Fill
BUD: 120 Days Room Temp
Fentanyl Citrate 400 mcg/200 mL + 0.1% Ropivacaine in 0.9% Sodium Chloride
NDC: 71139-5340-2
Bag for Injection (For Epidural Use)
250 mL Bag - 200 mL Fill
BUD: 120 Days Room Temp
Fentanyl Citrate 2500 mcg/50 mL
NDC: 71139-6030-1
CADD for Injection (Concentration 50 mcg/mL)
50 mL Reservoir - 50 mL Fill
BUD: 180 Days Room Temp
Hydromorphone HCl 20mg/100ml CADD for injection
NDC: 71139-0018-1
(Concentration 0.2mg/ml) in 0.9% Sodium Chloride
100 mL Reservoir - 100 mL Fill
BUD: 120 Days Room Temp
Oxytocin 30 Units in 0.9% Sodium Chloride
NDC: 71139-0012-1
Bag for Injection (Volume ~545 mL)
500 mL Bag
BUD: 120 Days Room Temp

About IntegraDose

We’re here to make a hospital work better at a time when it’s hard to make a hospital work at all.

IntegraDose started as a part of Fairview Pharmacy, a leader in health-system pharmacy innovation.  As part of a health system, we understand the ins and outs of sterile compounding and understand the importance of getting the most commonly compounded medications to patients as quickly, accurately and efficiently as possible.  At IntegraDose, we’ve reimagined the process to anticipate needs, minimize drug shortage impacts, provide better products and drive system standardization.  That helps hospitals deliver commonly compounded medications more efficiently, reduce their liability risk and realize savings that extend from the pharmacy all the way to the patient.

Committed to Quality

We use these products in our own hospitals first, and we are committed to the highest standards of quality and safety. We maintain compliance with all regulatory requirements and expectations including 21 Code of Federal Regulations, Parts 210 & 211 and Interim Guidance for Human Drug Compounding Outsourcing Facilities Under Section 503B of the FD&C Act.

State-of-the-art Facility

Our 503B compounding facility is designed to ensure the rooms, air, hoods, and staff are actively sampled during production and all process steps are well defined, monitored and reviewed. And each product our facility produces is validated through long term testing, each batch is sampled for potency, sterility and bacterial endotoxin and all medication batches are quarantined until successful sample results have been confirmed by external test labs.

Our People

Craig Else

COO, IntegraDose Compounding Services

Craig grew up in his dad’s community pharmacy.  He was a hospital pharmacy technician for 11 years, hospital staff pharmacist for 10 years, hospital manager/director for 10 years, and a health-system pharmacy director for 4 years. In addition, he been a long time Board Member and Past-President of both the Minnesota Society of Health-System Pharmacists and the Minnesota Pharmacists Association. His extensive experience in acute-care settings is what led him to start IntegraDose. 

Kimberly A Grandprey

Pharmaceutical Compounding QA Program Manager

Kimberly is the Pharmaceutical Compounding Quality Assurance Program Manager at IntegraDose. A University of Minnesota graduate, she has more than 30 years in the quality control and quality assurance fields and is— it’s fair to say — a proven expert in pharmaceutical manufacturing, medical device, and environmental testing areas including establishing and maintenance of FDA, EPA, ISO 9001 and ISO 17025 registrations, SOP/Documentation and Document Control, OOS/RCA investigation and CAPA Management. In other words, she knows Current Good Manufacturing Practice (cGMP) inside and out.

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