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Lyophilizer(US FAD and EU cGMP Approved )is widely used in pharmaceutical field. - details see: https://www.machineto.com/the-pharmaceutical-vaccine-vacuum-pharmaceutical-freeze-drying-machine-us-fda-eu-cgmp-approved-10306250

Lyophilizer

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Design and Manufacturing According to FDA&cGMP Standard

Detailed Product Description

1,Mainly applied for pharmaceutical industries blood , bacterin and antibiotics production.

2,The dryin capacity from 200KG to 400KG.
3,The machine has compact design to reduce the occupation of plant area.

4,Machine compliance with GMP, all the system has modular design, more easily for maintenance and operation,

and its best choice before mass production started.

Features
1,Compact design, Reliability running under high performance, vacuum or air filled stoppering,

Eutectic device detector are available.

2, Control system designed with multi-recipe, user can choose different recipe for different process.

3,The control system can automatically validate the machine performance before each production cycle,

Thus the safety for each production cycle can be ensured.

Customer Option
1,Eutectic point detector

2,Organic solvent collector.

3,Inter-shelf distance adjust mechanism

4,Vacuum or air filled stoppering (with pressure adjustable)

5,Auto moisture judgment on control system

6,CIP/SIP

7,Chamber isolation valve with mushroom/butterfly type.

8,Constant height loading

9,Chamber door with auto/manual lock

10,Chamber vacuum adjust function

Contamination prevention
1,There are numerous cleanliness and safety systems on offer;

2,We can supply product protection systems including automatic CIP (Clean-in-Place) and SIP (Sterilization-in Place) systems.

3,These prevent contamination and increase the productivity by allowing a reduction in the number of staff needed to operate the equipment.

4,Further, automatic WIT (Water Intrusion Test) of the venting filters ensures integrity and increases the availability of the unit.

Technique Date:

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